Speakers
Click on photographs for information on our speakers

A medical doctor who branched out into public life, Dr. Harsh Vardhan has an impeccable electoral record of 25 years, having been elected five successive times to the Delhi Legislative Assembly and serving two consecutive terms as a Member of Parliament to the Lok Sabha (House of Commons). His public life has been stellar and marked by outstanding achievements in health, education, law, science, technology, and the environment.
Dr. Harsh Vardhan’s engagement in the eradication of the dreaded disease Poliomyelitis from India has found overwhelming global appreciation. Subsequently, he has been at the forefront of the battle against tobacco and drug abuse and was instrumental in the enactment of several laws in India to tackle these problems. For his long-standing commitment to humanity, Dr. Harsh Vardhan has been the proud recipient of various national and international awards of repute.
Dr. Harsh Vardhan became Union Minister of Health and Family Welfare for the second time in 2019, and has been at the forefront of India’s response to the ongoing COVID-19 crisis. He is also known worldwide for reiterating India’s commitment to end TB by 2025, stating that it is high time for the international community to implement faster and more innovative global TB control measures in the fight against the disease.
Since March 2021, Minister Harsh Vardhan is the Chair of the Stop TB Partnership Board.
A medical doctor who branched out into public life, Dr. Harsh Vardhan has an impeccable electoral record of 25 years, having been elected five successive times to the Delhi Legislative Assembly and serving two consecutive terms as a Member of Parliament to the Lok Sabha (House of Commons). His public life has been stellar and marked by outstanding achievements in health, education, law, science, technology, and the environment.
Dr. Harsh Vardhan’s engagement in the eradication of the dreaded disease Poliomyelitis from India has found overwhelming global appreciation. Subsequently, he has been at the forefront of the battle against tobacco and drug abuse and was instrumental in the enactment of several laws in India to tackle these problems. For his long-standing commitment to humanity, Dr. Harsh Vardhan has been the proud recipient of various national and international awards of repute.
Dr. Harsh Vardhan became Union Minister of Health and Family Welfare for the second time in 2019, and has been at the forefront of India’s response to the ongoing COVID-19 crisis. He is also known worldwide for reiterating India’s commitment to end TB by 2025, stating that it is high time for the international community to implement faster and more innovative global TB control measures in the fight against the disease.
Since March 2021, Minister Harsh Vardhan is the Chair of the Stop TB Partnership Board.

Olivier Veran was born on April 22nd , 1980 in Saint-Martin d’Heres, in the lsere region, where he spent his all of his childhood and attended school. Son of an engineer and an English teacher, his calling for the field of medicine began at an early age. This was strengthened during his night job as an attendant in an elderly home, serving the most fragile, to finance his studies in Grenoble.
Sensitive to the working conditions of caregivers, assistants and interns in the hospitals of Grenoble, he became involved in union life. After completing his thesis on “Epileptic confusion in the elderly”, Olivier Veran became neurologist at the Grenoble-Alpes University Hospital.
As assistant Head of Clinic of the Intensive Care Unit for Vascular Neurology, he was responsible for patients suffering from cerebrovascular accidents. Subsequently, he managed the day clinic of the Neurological department, receiving over 3.000 patients each year.
His political commitment led him to the French National Assembly in 2012, as Member of Parliament for the 1st district of the Isere. Profoundly committed to equal access to healthcare, he devoted the majority of his parliamentary work to health policies and to the fight against poverty, resulting in him becoming General Rapporteur of the Social Affairs Committee.
To uphold his beliefs in the territory that he is so close to, and which is important to him, Olivier Veran was elected Regional Councilor of the Auvergne-Rh6ne-Alpes region in December 2015. Since December 2019 he chairs the group “La Republique En Marche” (the party of the presidential majority) in this assembly.
On February 16th, 2020, Olivier Veran was nominated Minister of Solidarity and Health. Olivier Veran is the father of two children and is passionate about music.
Olivier Veran was born on April 22nd , 1980 in Saint-Martin d’Heres, in the lsere region, where he spent his all of his childhood and attended school. Son of an engineer and an English teacher, his calling for the field of medicine began at an early age. This was strengthened during his night job as an attendant in an elderly home, serving the most fragile, to finance his studies in Grenoble.
Sensitive to the working conditions of caregivers, assistants and interns in the hospitals of Grenoble, he became involved in union life. After completing his thesis on “Epileptic confusion in the elderly”, Olivier Veran became neurologist at the Grenoble-Alpes University Hospital.
As assistant Head of Clinic of the Intensive Care Unit for Vascular Neurology, he was responsible for patients suffering from cerebrovascular accidents. Subsequently, he managed the day clinic of the Neurological department, receiving over 3.000 patients each year.
His political commitment led him to the French National Assembly in 2012, as Member of Parliament for the 1st district of the Isere. Profoundly committed to equal access to healthcare, he devoted the majority of his parliamentary work to health policies and to the fight against poverty, resulting in him becoming General Rapporteur of the Social Affairs Committee.
To uphold his beliefs in the territory that he is so close to, and which is important to him, Olivier Veran was elected Regional Councilor of the Auvergne-Rh6ne-Alpes region in December 2015. Since December 2019 he chairs the group “La Republique En Marche” (the party of the presidential majority) in this assembly.
On February 16th, 2020, Olivier Veran was nominated Minister of Solidarity and Health. Olivier Veran is the father of two children and is passionate about music.

Honorable Dr Sibongiseni Dhlomo is a medical doctor by profession and the Chairperson of the National Health Portfolio Committee in the National Assembly in Parliament. He is also the Chairperson of the national TB Caucus in South Africa. He is a seasoned politician and public health practitioner who has served as the MEC for Health in Kwa-Zulu Natal from 2009 – 2019.
He is a former member of Umkhonto Wesizwe and was incarcerated on Robben Island in the 1980’s.
He has also served in the South Africa National Defence and worked as an academic at the University of KwaZulu-Natal lecturing in Public Health.
Honorable Dr Sibongiseni Dhlomo is a medical doctor by profession and the Chairperson of the National Health Portfolio Committee in the National Assembly in Parliament. He is also the Chairperson of the national TB Caucus in South Africa. He is a seasoned politician and public health practitioner who has served as the MEC for Health in Kwa-Zulu Natal from 2009 – 2019.
He is a former member of Umkhonto Wesizwe and was incarcerated on Robben Island in the 1980’s.
He has also served in the South Africa National Defence and worked as an academic at the University of KwaZulu-Natal lecturing in Public Health.

Stéphanie Seydoux has been appointed French Ambassador for Global health in 2018, representing France in various international organizations (Global Fund, Unitaid…). She was involved in the 6th Global Fund replenishment conference in Lyon, in October 2019 and is currently active in the French multilateral response to the Covid crisis (in particular through ACT-A), which was developed alongside strengthening major health and development priorities such as health system strengthening, gender equality, the fight against pandemics for instance.
After starting her career at the Ministry of Foreign Affairs, Stéphanie Seydoux joined the General Inspectorate of Social Affairs (IGAS) in 2004. From 2007 to 2010, she was Head of Equality Promotion at the French Independent Equality Commission. From 2010 to 2013, she was Deputy Ambassador at the French Embassy in Kenya. She was head of the French Women’s rights department from 2014 to 2017.
Stéphanie Seydoux holds a master’s degree in literature from the University of Oxford, a graduate of the Paris Institute of Political Studies (Sciences Po) and is a former student of the National School of Administration (ENA) – promotion “Léopold Sédar Senghor”
Stéphanie Seydoux has been appointed French Ambassador for Global health in 2018, representing France in various international organizations (Global Fund, Unitaid…). She was involved in the 6th Global Fund replenishment conference in Lyon, in October 2019 and is currently active in the French multilateral response to the Covid crisis (in particular through ACT-A), which was developed alongside strengthening major health and development priorities such as health system strengthening, gender equality, the fight against pandemics for instance.
After starting her career at the Ministry of Foreign Affairs, Stéphanie Seydoux joined the General Inspectorate of Social Affairs (IGAS) in 2004. From 2007 to 2010, she was Head of Equality Promotion at the French Independent Equality Commission. From 2010 to 2013, she was Deputy Ambassador at the French Embassy in Kenya. She was head of the French Women’s rights department from 2014 to 2017.
Stéphanie Seydoux holds a master’s degree in literature from the University of Oxford, a graduate of the Paris Institute of Political Studies (Sciences Po) and is a former student of the National School of Administration (ENA) – promotion “Léopold Sédar Senghor”

Dr. Andersen-Nissen directs cellular immunology studies of specimens from HIV Vaccine Trials Network (HVTN) studies in Southern Africa. She holds a Senior Staff Scientist position at the Fred Hutchinson Cancer Research Center and is an Honourary Research Associate at the University of Cape Town in the Division of Medical Virology. Dr. Andersen-Nissen completed her PhD in immunology at the University of Washington in Seattle in June 2006 under the mentorship of Dr. Alan Aderem. She then pursued a postdoctoral fellowship in Dr. Julie McElrath’s laboratory at the Fred Hutchinson Cancer Research Center where she profiled innate immune responses induced by candidate HIV vaccines, providing new information about human immune responses to experimental adjuvants and viral vaccine vectors. Erica relocated to Cape Town in January 2013 to start CHIL and is studying innate and adaptive immune responses elicited by HIV and TB vaccines in Southern African populations to identify immune correlates of risk and protection.
Dr. Andersen-Nissen directs cellular immunology studies of specimens from HIV Vaccine Trials Network (HVTN) studies in Southern Africa. She holds a Senior Staff Scientist position at the Fred Hutchinson Cancer Research Center and is an Honourary Research Associate at the University of Cape Town in the Division of Medical Virology. Dr. Andersen-Nissen completed her PhD in immunology at the University of Washington in Seattle in June 2006 under the mentorship of Dr. Alan Aderem. She then pursued a postdoctoral fellowship in Dr. Julie McElrath’s laboratory at the Fred Hutchinson Cancer Research Center where she profiled innate immune responses induced by candidate HIV vaccines, providing new information about human immune responses to experimental adjuvants and viral vaccine vectors. Erica relocated to Cape Town in January 2013 to start CHIL and is studying innate and adaptive immune responses elicited by HIV and TB vaccines in Southern African populations to identify immune correlates of risk and protection.

Álvaro Borges is a physician-scientist educated in Brazil, the United Kingdom and Denmark. He has an MSc in Tropical and Infectious Diseases (Liverpool School of Tropical Medicine 2011) and a PhD in Immunology and Infectious Diseases (University of Copenhagen 2015). He joined the Center for Vaccine Research at Statens Serum Institut as chief medical officer to work on clinical trials testing new candidate vaccines in humans. He has been actively involved in 1) design and coordination of clinical trials and research projects primarily within vaccines, 2) studies of pathogen mechanisms and natural immunity / vaccine immunity in human cohorts, 3) clinical data interpretation, preparation of scientific manuscripts and presentations at international meetings and 4) fundraising for clinical trials.
Álvaro Borges is a physician-scientist educated in Brazil, the United Kingdom and Denmark. He has an MSc in Tropical and Infectious Diseases (Liverpool School of Tropical Medicine 2011) and a PhD in Immunology and Infectious Diseases (University of Copenhagen 2015). He joined the Center for Vaccine Research at Statens Serum Institut as chief medical officer to work on clinical trials testing new candidate vaccines in humans. He has been actively involved in 1) design and coordination of clinical trials and research projects primarily within vaccines, 2) studies of pathogen mechanisms and natural immunity / vaccine immunity in human cohorts, 3) clinical data interpretation, preparation of scientific manuscripts and presentations at international meetings and 4) fundraising for clinical trials.

Muhwa Jeremiah Chakaya, is a Professor, Global Respiratory Health, at the department of clinical sciences, Liverpool School of Tropical Medicine. Prof. Chakaya hails from Kenya where he was born and educated and where he practices and teaches respiratory medicine. He graduated from the University of Nairobi with a basic degree in medicine and surgery (MBChB) in 1985 and a master’s degree in internal medicine (M.Med) in 1992. He then went on to study lung medicine at the National Lung and Heart Institute, University of London at the Royal Brompton Hospital and at the Kyorin University Hospital in Tokyo, Japan. Prof. Chakaya worked as a TB and Lung disease researcher at the Centre for Respiratory Diseases Research at the Kenya Medical Research Institute and later served as the TB Program Manager at the Ministry of Health between 2003 and 2006. At the international level, Prof. Chakaya has held several positions including, Vice Chair of the Stop TB Partnership Coordinating Board, Chair of the Strategic and Technical Advisory Group for TB (STAG-TB ) of the World Health Organization (WHO), Chair of the Global Fund’s Technical Review Panel (TRP) and President of the International Union Against Tuberculosis and Lung Disease ( the Union). Prof. Chakaya is a founder member of the Respiratory Society of Kenya (ReSoK) and has remained closely engaged with this organization. He is a member of the Pan African Thoracic Society and serves in the executive committee of this organization. He has a honorary teaching position at the school of medicine, Kenyatta University, Nairobi, Kenya.
Muhwa Jeremiah Chakaya, is a Professor, Global Respiratory Health, at the department of clinical sciences, Liverpool School of Tropical Medicine. Prof. Chakaya hails from Kenya where he was born and educated and where he practices and teaches respiratory medicine. He graduated from the University of Nairobi with a basic degree in medicine and surgery (MBChB) in 1985 and a master’s degree in internal medicine (M.Med) in 1992. He then went on to study lung medicine at the National Lung and Heart Institute, University of London at the Royal Brompton Hospital and at the Kyorin University Hospital in Tokyo, Japan. Prof. Chakaya worked as a TB and Lung disease researcher at the Centre for Respiratory Diseases Research at the Kenya Medical Research Institute and later served as the TB Program Manager at the Ministry of Health between 2003 and 2006. At the international level, Prof. Chakaya has held several positions including, Vice Chair of the Stop TB Partnership Coordinating Board, Chair of the Strategic and Technical Advisory Group for TB (STAG-TB ) of the World Health Organization (WHO), Chair of the Global Fund’s Technical Review Panel (TRP) and President of the International Union Against Tuberculosis and Lung Disease ( the Union). Prof. Chakaya is a founder member of the Respiratory Society of Kenya (ReSoK) and has remained closely engaged with this organization. He is a member of the Pan African Thoracic Society and serves in the executive committee of this organization. He has a honorary teaching position at the school of medicine, Kenyatta University, Nairobi, Kenya.

Prof. Gavin Churchyard (MBBCh), MMED (Int Med), FCP (SA), FRCP (Edin), PhD) is a specialist physician, internationally renowned for his contributions in tuberculosis (TB) research. Prof Churchyard is the founder and Group Chief Executive Officer of the Aurum Institute, an independent, not for profit, proudly South African, public benefit organization that focuses on TB and HIV technical assistance, service delivery, and research. Prof Churchyard is an Honorary Professor at the University of Witwatersrand, University of Cape Town and the Department of Medicine in the Vanderbilt University School of Medicine. Prof Churchyard is the Chair of the AIDS Clinical Trials Group (ACTG) Transformative Science Group for TB, Chair of the NIH/DIADS funded Cross-network TB vaccine and Immunology Working Group, and a member of the ACTG Scientific Advisory Steering Committee (SASC). He has extensive clinical trials experience and has conducted numerous TB treatment, TB vaccine, TB preventive therapy, TB diagnostics and Host Directed Therapy for TB trials. Prof Churchyard’s investigator-initiated studies has involved large, multisite and often complex studies in South Africa and internationally. Prof Churchyard has published widely in the fields of TB and HIV.
Prof. Gavin Churchyard (MBBCh), MMED (Int Med), FCP (SA), FRCP (Edin), PhD) is a specialist physician, internationally renowned for his contributions in tuberculosis (TB) research. Prof Churchyard is the founder and Group Chief Executive Officer of the Aurum Institute, an independent, not for profit, proudly South African, public benefit organization that focuses on TB and HIV technical assistance, service delivery, and research. Prof Churchyard is an Honorary Professor at the University of Witwatersrand, University of Cape Town and the Department of Medicine in the Vanderbilt University School of Medicine. Prof Churchyard is the Chair of the AIDS Clinical Trials Group (ACTG) Transformative Science Group for TB, Chair of the NIH/DIADS funded Cross-network TB vaccine and Immunology Working Group, and a member of the ACTG Scientific Advisory Steering Committee (SASC). He has extensive clinical trials experience and has conducted numerous TB treatment, TB vaccine, TB preventive therapy, TB diagnostics and Host Directed Therapy for TB trials. Prof Churchyard’s investigator-initiated studies has involved large, multisite and often complex studies in South Africa and internationally. Prof Churchyard has published widely in the fields of TB and HIV.

Professor Cooper received her undergraduate degree from University College, London and her Doctoral degree from The London School of Hygiene and Tropical Medicine UK, where she investigated the interaction between macrophages and protozoan parasites of the genus Leishmania. Moving to the National Institutes of Health in Bethesda, Maryland, US she expanded her investigation of leishmaniasis to include the T cell response of patients suffering from cutaneous, mucocutaneous and visceral forms of this disease. She then moved to the Mycobacterial Research Labs at Colorado State University and began studying the protective immune response to Mycobacterium tuberculosis. Prior to her move to the University of Leicester she was at the Trudeau Institute, Inc. for 12 years where she held the E.L. Trudeau Chair. The underlying theme of Professor Cooper’s work is the definition of the mechanisms which mediate initiation, expression and regulation of immunity within the lung.
Professor Cooper received her undergraduate degree from University College, London and her Doctoral degree from The London School of Hygiene and Tropical Medicine UK, where she investigated the interaction between macrophages and protozoan parasites of the genus Leishmania. Moving to the National Institutes of Health in Bethesda, Maryland, US she expanded her investigation of leishmaniasis to include the T cell response of patients suffering from cutaneous, mucocutaneous and visceral forms of this disease. She then moved to the Mycobacterial Research Labs at Colorado State University and began studying the protective immune response to Mycobacterium tuberculosis. Prior to her move to the University of Leicester she was at the Trudeau Institute, Inc. for 12 years where she held the E.L. Trudeau Chair. The underlying theme of Professor Cooper’s work is the definition of the mechanisms which mediate initiation, expression and regulation of immunity within the lung.

Professor Nigel Curtis is a paediatric infectious diseases physician and clinician scientist. He is Professor of Paediatric Infectious Diseases at the University of Melbourne, Leader of the Infectious Diseases Research Group at the Murdoch Children’s Research Institute, and Head of Infectious Diseases at The Royal Children’s Hospital Melbourne.
He is the Chief Principal Investigator of The BRACE Trial, a randomised controlled trial of BCG vaccination to reduce the impact of COVID-19 in healthcare workers that has recruited in 34 sites in three continents worldwide.
Professor Nigel Curtis is a paediatric infectious diseases physician and clinician scientist. He is Professor of Paediatric Infectious Diseases at the University of Melbourne, Leader of the Infectious Diseases Research Group at the Murdoch Children’s Research Institute, and Head of Infectious Diseases at The Royal Children’s Hospital Melbourne.
He is the Chief Principal Investigator of The BRACE Trial, a randomised controlled trial of BCG vaccination to reduce the impact of COVID-19 in healthcare workers that has recruited in 34 sites in three continents worldwide.

Dr. Sajjad A Desai, is a graduate (MBBS) and post‐graduate (MD) of Dr V. M. Medical College, Solapur with specialization in Clinical Pharmacology. He joined Serum Institute of India Ltd. (SIIL), Pune in 2006 and is working as Deputy Medical Director. After post‐graduation in 2001, he has worked in several pharmaceutical companies in R & D ‐ Clinical Research. Since 2006, he is working with Serum Institute of India Pvt Ltd and is involved in clinical development of new vaccines and biologicals as well pharmacovigilance activities. He has publications in peer reviewed scientific journals and is a life member of the Indian Society for Clinical Research.
Dr. Sajjad A Desai, is a graduate (MBBS) and post‐graduate (MD) of Dr V. M. Medical College, Solapur with specialization in Clinical Pharmacology. He joined Serum Institute of India Ltd. (SIIL), Pune in 2006 and is working as Deputy Medical Director. After post‐graduation in 2001, he has worked in several pharmaceutical companies in R & D ‐ Clinical Research. Since 2006, he is working with Serum Institute of India Pvt Ltd and is involved in clinical development of new vaccines and biologicals as well pharmacovigilance activities. He has publications in peer reviewed scientific journals and is a life member of the Indian Society for Clinical Research.

Dr. Mustafa Diken received his Ph.D. in tumor immunology from Johannes Gutenberg University, Mainz and is currently serving as Vice President Vaccines & Immunology at BioNTech SE. His research focuses on the development of novel cancer and infectious disease vaccines based on antigen-encoding messenger RNA (mRNA). His research led to novel mRNA vaccines which are currently being tested in several clinical trials.
Dr. Mustafa Diken received his Ph.D. in tumor immunology from Johannes Gutenberg University, Mainz and is currently serving as Vice President Vaccines & Immunology at BioNTech SE. His research focuses on the development of novel cancer and infectious disease vaccines based on antigen-encoding messenger RNA (mRNA). His research led to novel mRNA vaccines which are currently being tested in several clinical trials.

Dr. Lucica Ditiu, Executive Director of the Stop TB Partnership is a Romanian physician, accomplished professional and leader in the global fight against tuberculosis (TB) and other communicable diseases. Dr. Ditiu is driven by the firm belief that we should “leave no one behind” and is one of the strongest advocates within the international community in the fight against tuberculosis. A firm believer in innovation, flexibility, change, breaking the rules and thinking out of the box, Dr. Ditiu is dedicated to driving political commitment and engagement to accelerate the efforts to End TB.
Dr. Lucica Ditiu, Executive Director of the Stop TB Partnership is a Romanian physician, accomplished professional and leader in the global fight against tuberculosis (TB) and other communicable diseases. Dr. Ditiu is driven by the firm belief that we should “leave no one behind” and is one of the strongest advocates within the international community in the fight against tuberculosis. A firm believer in innovation, flexibility, change, breaking the rules and thinking out of the box, Dr. Ditiu is dedicated to driving political commitment and engagement to accelerate the efforts to End TB.

Professor Gordon Dougan F Med Sci FRS, who is a Professor in the Department of Medicine at Cambridge University, is an internationally recognised expert in vaccinology, global health and infections. He was Head of Pathogens at The Wellcome Sanger Institute (WTSI) and worked in the pharmaceutical industry. He studies the molecular basis of infection with a strong emphasis on pathogenic mechanisms/immunity, genomics, disease tracking and antibiotic resistance. He has a particular interest in using genomics to study the evolution of Salmonella enterica serovar Typhi, the cause of typhoid.
Before moving to the WTSI he was the founding Director of the Centre for Molecular Microbiology and Infection at Imperial College London and a Professor of Biochemistry. He is a member of EMBO, a Fellow of the Academy of Medical Sciences and a Fellow of the Royal Society. He has received awards nationally and internationally for his work, including the Albert B Sabin Gold Medal for his work on Affordable Vaccines. He received his B Sc and Ph.D. from the University of Sussex and conducted postdoctoral studies at the University of Washington (Seattle) in the laboratory of the Lasker Prize winner Stanley Falkow. During his work in industry developing novel vaccines at an internationally renowned multi-national company now part of GSK and is a founder of VHSquared and Microbiotica. He is currently a Head of the Infection Health Challenge area at Wellcome.
Professor Gordon Dougan F Med Sci FRS, who is a Professor in the Department of Medicine at Cambridge University, is an internationally recognised expert in vaccinology, global health and infections. He was Head of Pathogens at The Wellcome Sanger Institute (WTSI) and worked in the pharmaceutical industry. He studies the molecular basis of infection with a strong emphasis on pathogenic mechanisms/immunity, genomics, disease tracking and antibiotic resistance. He has a particular interest in using genomics to study the evolution of Salmonella enterica serovar Typhi, the cause of typhoid.
Before moving to the WTSI he was the founding Director of the Centre for Molecular Microbiology and Infection at Imperial College London and a Professor of Biochemistry. He is a member of EMBO, a Fellow of the Academy of Medical Sciences and a Fellow of the Royal Society. He has received awards nationally and internationally for his work, including the Albert B Sabin Gold Medal for his work on Affordable Vaccines. He received his B Sc and Ph.D. from the University of Sussex and conducted postdoctoral studies at the University of Washington (Seattle) in the laboratory of the Lasker Prize winner Stanley Falkow. During his work in industry developing novel vaccines at an internationally renowned multi-national company now part of GSK and is a founder of VHSquared and Microbiotica. He is currently a Head of the Infection Health Challenge area at Wellcome.

Shiva Dustdar has over 25 years of experience in the financial industry working for large private and public institutions in New York, London and Luxembourg. Since joining EIB in 2003, she has worked in risk management, lending and investing in innovative companies and currently heads the Innovation Finance Advisory (IFA) Division in the EIB which she was tasked to set up in 2013. IFA has 2 units covering project advisory and thematic finance providing access to finance advice to public and private entities, performing market studies and developing new financial products to meet the financing needs across the innovation spectrum to support smart, green and healthy growth.
Shiva started her career in 1993 at J.P. Morgan Investment Banking in New York working in M&A, Project Finance and Emerging Markets before joining Fitch Rating Agency in 1999 to set up its European High Yield rating business.
Shiva holds a BA in Economics from Columbia University and an Executive MBA from London Business School (LBS). Shiva co-founded the European High Yield Association (EHYA), which is now part of the Association for Financial Markets in Europe (AFME) and was nominated to Top 50 Women in Credit by Credit Magazine in 2006. She is a regular speaker on innovation and impact financing, gender smart investing, digital and green financing and actively engaged in networks that promote sustainable and mission oriented financing.
Shiva Dustdar has over 25 years of experience in the financial industry working for large private and public institutions in New York, London and Luxembourg. Since joining EIB in 2003, she has worked in risk management, lending and investing in innovative companies and currently heads the Innovation Finance Advisory (IFA) Division in the EIB which she was tasked to set up in 2013. IFA has 2 units covering project advisory and thematic finance providing access to finance advice to public and private entities, performing market studies and developing new financial products to meet the financing needs across the innovation spectrum to support smart, green and healthy growth.
Shiva started her career in 1993 at J.P. Morgan Investment Banking in New York working in M&A, Project Finance and Emerging Markets before joining Fitch Rating Agency in 1999 to set up its European High Yield rating business.
Shiva holds a BA in Economics from Columbia University and an Executive MBA from London Business School (LBS). Shiva co-founded the European High Yield Association (EHYA), which is now part of the Association for Financial Markets in Europe (AFME) and was nominated to Top 50 Women in Credit by Credit Magazine in 2006. She is a regular speaker on innovation and impact financing, gender smart investing, digital and green financing and actively engaged in networks that promote sustainable and mission oriented financing.

Emilio A. Emini, Ph.D. is the Director of the Tuberculosis and HIV Program at the Bill & Melinda Gates Foundation. He is also a Board member of the Gates Medical Research Institute. Emilio joined the foundation in 2015 following a greater than 30-year career in the biopharmaceutical industry during which he held multiple senior positions in anti-infectives and vaccines R&D. At the Merck Research Laboratories, from 1983 to 2004, Emilio led the biological research that developed the first of the highly active antiretroviral therapies for HIV, and he led multiple teams involved in vaccine development programs including the recombinant hepatitis B, inactivated hepatitis A, the human papillomavirus, varicella, and rotavirus vaccine programs. Following a two-year leave from the industry at the International AIDS Vaccine Initiative, Emilio joined Wyeth/Pfizer Inc. as the Senior Vice President of Vaccine R&D where he led the development of the Prevenar 13 vaccine for prevention of pneumococcal disease. In addition to his present role at the foundation, Emilio serves as an advisor to the COVID vaccine programs of the U.S. Department of Health and Human Services.
Emilio A. Emini, Ph.D. is the Director of the Tuberculosis and HIV Program at the Bill & Melinda Gates Foundation. He is also a Board member of the Gates Medical Research Institute. Emilio joined the foundation in 2015 following a greater than 30-year career in the biopharmaceutical industry during which he held multiple senior positions in anti-infectives and vaccines R&D. At the Merck Research Laboratories, from 1983 to 2004, Emilio led the biological research that developed the first of the highly active antiretroviral therapies for HIV, and he led multiple teams involved in vaccine development programs including the recombinant hepatitis B, inactivated hepatitis A, the human papillomavirus, varicella, and rotavirus vaccine programs. Following a two-year leave from the industry at the International AIDS Vaccine Initiative, Emilio joined Wyeth/Pfizer Inc. as the Senior Vice President of Vaccine R&D where he led the development of the Prevenar 13 vaccine for prevention of pneumococcal disease. In addition to his present role at the foundation, Emilio serves as an advisor to the COVID vaccine programs of the U.S. Department of Health and Human Services.

Dr. Emily Erbelding is an infectious disease physician who directs the Division of Microbiology and Infectious Diseases at the National Institute of Allergy and Infectious Diseases at the National Institutes of Health. As DMID director, she oversees a research portfolio of basic, translational, and clinical research in infectious diseases that exceeds $2B annually. NIAID continues to lead the research response to emerging and re-emerging infectious diseases. Prior to her role as DMID director, she served as Deputy Director in the Division of AIDS at NIAID.
Dr. Emily Erbelding is an infectious disease physician who directs the Division of Microbiology and Infectious Diseases at the National Institute of Allergy and Infectious Diseases at the National Institutes of Health. As DMID director, she oversees a research portfolio of basic, translational, and clinical research in infectious diseases that exceeds $2B annually. NIAID continues to lead the research response to emerging and re-emerging infectious diseases. Prior to her role as DMID director, she served as Deputy Director in the Division of AIDS at NIAID.

Dr. Michael Gerner obtained his Ph.D. in Immunology in 2009 at the University of Minnesota, studying anti-tumor immune responses. He next completed his postdoc at the NIH, where he developed and employed cutting-edge quantitative imaging tools to study the organization of immune cells in lymphoid tissues. In 2015, Dr. Gerner joined the University of Washington, Department of Immunology as Assistant Professor. His lab investigates how local tissue microenvironments shape the generation of innate and adaptive immune responses during vaccination, infection and cancer. The laboratory also continues to develop advanced image analysis platforms. Current efforts utilize these microscopy tools to better understand correlates of vaccine-mediated protection against Mycobacterium tuberculosis infection in mice and across species.
Dr. Michael Gerner obtained his Ph.D. in Immunology in 2009 at the University of Minnesota, studying anti-tumor immune responses. He next completed his postdoc at the NIH, where he developed and employed cutting-edge quantitative imaging tools to study the organization of immune cells in lymphoid tissues. In 2015, Dr. Gerner joined the University of Washington, Department of Immunology as Assistant Professor. His lab investigates how local tissue microenvironments shape the generation of innate and adaptive immune responses during vaccination, infection and cancer. The laboratory also continues to develop advanced image analysis platforms. Current efforts utilize these microscopy tools to better understand correlates of vaccine-mediated protection against Mycobacterium tuberculosis infection in mice and across species.

Dr. Hannah P. Gideon received her bachelor’s and master’s degree in Medical Microbiology in India and her PhD from the University of Cape Town, South Africa. For her post-doctoral research, she joined Prof. JoAnne Flynn’s group at the University of Pittsburgh School of Medicine, USA, to investigate T cell responses at the local (i.e., granuloma) and systemic level and whole blood transcriptional signatures of Mtb infection in NHP model. Dr. Gideon is currently a Research Assistant Professor in the Department of Microbiology and Molecular Genetics at the University of Pittsburgh School of Medicine and she leads studies interrogating immune repertories at the granulomas level using single-cell RNA sequencing in NHPs.
Dr. Hannah P. Gideon received her bachelor’s and master’s degree in Medical Microbiology in India and her PhD from the University of Cape Town, South Africa. For her post-doctoral research, she joined Prof. JoAnne Flynn’s group at the University of Pittsburgh School of Medicine, USA, to investigate T cell responses at the local (i.e., granuloma) and systemic level and whole blood transcriptional signatures of Mtb infection in NHP model. Dr. Gideon is currently a Research Assistant Professor in the Department of Microbiology and Molecular Genetics at the University of Pittsburgh School of Medicine and she leads studies interrogating immune repertories at the granulomas level using single-cell RNA sequencing in NHPs.

Ann M. Ginsberg, M.D., Ph.D., is Deputy Director, TB Vaccines in the Global Health Division of the Bill & Melinda Gates Foundation. Dr. Ginsberg has conducted and led TB research and product development programs for 25 years, including 15 years leading and designing clinical strategy for development of TB vaccines and drug regimens for the developing world. She previously served as the Chief, Respiratory Diseases Branch, NIAID, NIH; as Director, Project Management at Merck Research Laboratories; as Chief Medical Officer at the Global Alliance for TB Drug Development; as Chief Medical Officer at Aeras and as Senior Technical Advisor at IAVI. In these roles, she oversaw the early clinical development program of Pretomanid® and two recent, positive TB vaccine efficacy trials – of BCG revaccination and M72/AS01E. Dr. Ginsberg has served on numerous national and international advisory committees on vaccines and global health, including the U.S. National Vaccine Advisory Committee. Her undergraduate degree is from Harvard University, her Ph.D. in Molecular Biology from Washington University and her M.D. from Columbia University.
Ann M. Ginsberg, M.D., Ph.D., is Deputy Director, TB Vaccines in the Global Health Division of the Bill & Melinda Gates Foundation. Dr. Ginsberg has conducted and led TB research and product development programs for 25 years, including 15 years leading and designing clinical strategy for development of TB vaccines and drug regimens for the developing world. She previously served as the Chief, Respiratory Diseases Branch, NIAID, NIH; as Director, Project Management at Merck Research Laboratories; as Chief Medical Officer at the Global Alliance for TB Drug Development; as Chief Medical Officer at Aeras and as Senior Technical Advisor at IAVI. In these roles, she oversaw the early clinical development program of Pretomanid® and two recent, positive TB vaccine efficacy trials – of BCG revaccination and M72/AS01E. Dr. Ginsberg has served on numerous national and international advisory committees on vaccines and global health, including the U.S. National Vaccine Advisory Committee. Her undergraduate degree is from Harvard University, her Ph.D. in Molecular Biology from Washington University and her M.D. from Columbia University.

Ingrid Murillo Jelsbak is since January 2016 the Clinical Research Director at Biofabri, which belongs to Zendal Group at Porriño, a Spanish biopharmaceutical Business Group, focussed on the development manufacturing and marketing of vaccines as well as biological and pharmaceutical products for both human and animal health.
After finishing studies in Biology, with specialization in zoology at Universidad Complutense, Madrid, she started her carrier at Pharma Industry where she has been for the last 20 years exercising several responsibilities mainly in the Clinical Research area at Pharmaceutical companies and Contract Research Organizations (CROs) covering several responsibilities at national and international level, reaching the Managing Direction level for the Iberian region at Chiltern International, a UK-based international CRO, during six years.
Ingrid Murillo Jelsbak is since January 2016 the Clinical Research Director at Biofabri, which belongs to Zendal Group at Porriño, a Spanish biopharmaceutical Business Group, focussed on the development manufacturing and marketing of vaccines as well as biological and pharmaceutical products for both human and animal health.
After finishing studies in Biology, with specialization in zoology at Universidad Complutense, Madrid, she started her carrier at Pharma Industry where she has been for the last 20 years exercising several responsibilities mainly in the Clinical Research area at Pharmaceutical companies and Contract Research Organizations (CROs) covering several responsibilities at national and international level, reaching the Managing Direction level for the Iberian region at Chiltern International, a UK-based international CRO, during six years.

Having a biomedical background with a specialization in immunology, my main interest is to understand the human immune system in health and disease. Over the last decade my group has been working on host immunity towards tuberculosis (TB). TB biomarkers are one of the key subjects we have been working on, including bioprofiling of clinical samples. In addition, we have been interested in cellular immunity towards Mycobacterium tuberculosis (Mtb). My group aims to unravel the pathophysiological role of cellular immune responses in the combat against Mtb. We focus in particular on HLA-E restricted CD8+T-cells, B-cells and more recently also monocyte subsets. We aim to combine clinical data and samples with functional immunological characterization of the responses.
Having a biomedical background with a specialization in immunology, my main interest is to understand the human immune system in health and disease. Over the last decade my group has been working on host immunity towards tuberculosis (TB). TB biomarkers are one of the key subjects we have been working on, including bioprofiling of clinical samples. In addition, we have been interested in cellular immunity towards Mycobacterium tuberculosis (Mtb). My group aims to unravel the pathophysiological role of cellular immune responses in the combat against Mtb. We focus in particular on HLA-E restricted CD8+T-cells, B-cells and more recently also monocyte subsets. We aim to combine clinical data and samples with functional immunological characterization of the responses.

Professor Kang conducts inter-disciplinary research on enteric infections and child health. Her team has evaluated vaccines in pre-clinical and clinical phase 1-3 studies for enteric infections. She is a member of many WHO advisory committees, is the vice-Chair of the Board of Coalition of Epidemic Preparedness Innovations and chairs the Immunization Technical Advisory Group for the WHO’s South East Asian Region.
Professor Kang conducts inter-disciplinary research on enteric infections and child health. Her team has evaluated vaccines in pre-clinical and clinical phase 1-3 studies for enteric infections. She is a member of many WHO advisory committees, is the vice-Chair of the Board of Coalition of Epidemic Preparedness Innovations and chairs the Immunization Technical Advisory Group for the WHO’s South East Asian Region.

Evaline Kibuchi is a global health advocate with a key focus on Tuberculosis (TB) with over ten years in TB advocacy. Since 2015, she has served as the Chief National Coordinator, Stop TB Partnership-Kenya. She previously worked with International AIDS Vaccine Initiative in Community preparedness for the HIV vaccines trials. She is also the African Director of African Parliamentary TB caucus and a member of the Civil Society Task force the WHO TB team and a member of Access to Covid Tools Accelerator (ACT-A) an advocacy group that pushes for covid tools and other services.
She is a graduate of Bachelor of Arts from the University of Nairobi and completing her Masters of Public Health in Moi University. She holds Post Graduate Diploma in Mass Communication and journalism from the University of Nairobi, a Graduate Certificate, Participatory Monitoring and Evaluation, Center for finance and Project Management and Certificate in Resource mobilization and a certificate in policy development and advocacy for global health from the University of Washington.
She is the Chair, board of Directors, WACI Health a South African based Global Health advocacy organization. She is also the Vice Chair, Aids Healthcare Foundation, which is also a global advocacy organization based in the US.
Evaline Kibuchi is a global health advocate with a key focus on Tuberculosis (TB) with over ten years in TB advocacy. Since 2015, she has served as the Chief National Coordinator, Stop TB Partnership-Kenya. She previously worked with International AIDS Vaccine Initiative in Community preparedness for the HIV vaccines trials. She is also the African Director of African Parliamentary TB caucus and a member of the Civil Society Task force the WHO TB team and a member of Access to Covid Tools Accelerator (ACT-A) an advocacy group that pushes for covid tools and other services.
She is a graduate of Bachelor of Arts from the University of Nairobi and completing her Masters of Public Health in Moi University. She holds Post Graduate Diploma in Mass Communication and journalism from the University of Nairobi, a Graduate Certificate, Participatory Monitoring and Evaluation, Center for finance and Project Management and Certificate in Resource mobilization and a certificate in policy development and advocacy for global health from the University of Washington.
She is the Chair, board of Directors, WACI Health a South African based Global Health advocacy organization. She is also the Vice Chair, Aids Healthcare Foundation, which is also a global advocacy organization based in the US.

Dr Anastasia Koch is the co-founder and co-director of Eh!woza. The organisation was established in 2013 as an informal collaboration between researchers at the Institute of Infectious Disease and Molecular Medicine (IDM), conceptual artist Ed Young, social scientists, and young people from Khayelitsha, a peri-urban township in Cape Town. In 2020, Eh!woza was awarded a Wellcome Trust Discretionary Award in Public Engagement, which facilitated the organisation’s transition into an independent NPO. Eh!woza enlists beneficiaries as active partners and facilitate access to accurate information while igniting frank conversations, storytelling and representation of health and disease. Long-term goals are to encourage positive health-seeking behaviour, engender trust, and decrease stigma. Before working fulltime on Eh!woza, Anastasia was a junior research fellow at the Molecular Mycobacteriology Research Unit (IDM, UCT), which she maintains in a parttime position. Anastasia’s biomedical research interests involve using genomics to understand the transmission and pathobiology of Mycobacterium tuberculosis.
Dr Anastasia Koch is the co-founder and co-director of Eh!woza. The organisation was established in 2013 as an informal collaboration between researchers at the Institute of Infectious Disease and Molecular Medicine (IDM), conceptual artist Ed Young, social scientists, and young people from Khayelitsha, a peri-urban township in Cape Town. In 2020, Eh!woza was awarded a Wellcome Trust Discretionary Award in Public Engagement, which facilitated the organisation’s transition into an independent NPO. Eh!woza enlists beneficiaries as active partners and facilitate access to accurate information while igniting frank conversations, storytelling and representation of health and disease. Long-term goals are to encourage positive health-seeking behaviour, engender trust, and decrease stigma. Before working fulltime on Eh!woza, Anastasia was a junior research fellow at the Molecular Mycobacteriology Research Unit (IDM, UCT), which she maintains in a parttime position. Anastasia’s biomedical research interests involve using genomics to understand the transmission and pathobiology of Mycobacterium tuberculosis.

Dr. Jim Kublin is currently Executive Director of the COVID-19 Prevention Network and HIV Vaccine Trials Network based at Fred Hutchinson Cancer Research Center. He is also the Medical Director of the Seattle Malaria Clinical Trials Center, a translational research center established by Fred Hutch and the Seattle Children’s Research Institute to test experimental malaria vaccines and drugs in human clinical trials. Jim is also a Clinical Professor in the Department of Global Health at the University of Washington and runs a lab focused on the impact of the microbiome on vaccine responses. Jim has conducted extensive research on HIV, TB and malaria in South America, SE Asia, and Africa, including clinical trials of novel therapies and vaccines. The Gates Foundation awarded Jim a Grand Challenges Exploration award to apply high-throughput system analyses to malaria vaccine development. Before moving to Seattle, Jim was Director, HIV Vaccines – Infectious Diseases, for Merck & Co., Inc where he played a key role in the development and implementation of HIV vaccine studies, overseeing the coordination of clinical assays, site identification and development, government and ethical approvals and providing guidance on vaccine policy issues. Jim completed his B.S. and M.D. at Georgetown University and received his M.P.H. and completed a residency in Preventive Medicine at Johns Hopkins University. Jim continued work in vaccine development and molecular epidemiology while attending the University of Maryland’s School of Medicine for his fellowship in Vaccinology at the Center for Vaccine Development.
Dr. Jim Kublin is currently Executive Director of the COVID-19 Prevention Network and HIV Vaccine Trials Network based at Fred Hutchinson Cancer Research Center. He is also the Medical Director of the Seattle Malaria Clinical Trials Center, a translational research center established by Fred Hutch and the Seattle Children’s Research Institute to test experimental malaria vaccines and drugs in human clinical trials. Jim is also a Clinical Professor in the Department of Global Health at the University of Washington and runs a lab focused on the impact of the microbiome on vaccine responses. Jim has conducted extensive research on HIV, TB and malaria in South America, SE Asia, and Africa, including clinical trials of novel therapies and vaccines. The Gates Foundation awarded Jim a Grand Challenges Exploration award to apply high-throughput system analyses to malaria vaccine development. Before moving to Seattle, Jim was Director, HIV Vaccines – Infectious Diseases, for Merck & Co., Inc where he played a key role in the development and implementation of HIV vaccine studies, overseeing the coordination of clinical assays, site identification and development, government and ethical approvals and providing guidance on vaccine policy issues. Jim completed his B.S. and M.D. at Georgetown University and received his M.P.H. and completed a residency in Preventive Medicine at Johns Hopkins University. Jim continued work in vaccine development and molecular epidemiology while attending the University of Maryland’s School of Medicine for his fellowship in Vaccinology at the Center for Vaccine Development.

Luciana C.C. Leite, has PhD in Biochemistry from the Universidade de São Paulo (USP). She was hired in 1987 at Instituto Butantan, at the Centro de Biotecnologia, changing to vaccine development following a Pos-Doc at Institut Pasteur. She has worked on the molecular biotechnology for development of vaccines, especially vaccines based on recombinant BCG. She has been Director of the Centro de Biotecnologia and Vice-President of Fundação Butantan. She is currently Senior Researcher at the Molecular Biotechnology laboratory of the Laboratório de Desenvolvimento de Vacinas, having over 120 papers in peer-reviewed journals and several patents. She is member of the Academic Management Board of the master program of the Leading International Vaccinology Education of Erasmus/European Union and of the Ethics Committee for Research in Humans of USP.
Luciana C.C. Leite, has PhD in Biochemistry from the Universidade de São Paulo (USP). She was hired in 1987 at Instituto Butantan, at the Centro de Biotecnologia, changing to vaccine development following a Pos-Doc at Institut Pasteur. She has worked on the molecular biotechnology for development of vaccines, especially vaccines based on recombinant BCG. She has been Director of the Centro de Biotecnologia and Vice-President of Fundação Butantan. She is currently Senior Researcher at the Molecular Biotechnology laboratory of the Laboratório de Desenvolvimento de Vacinas, having over 120 papers in peer-reviewed journals and several patents. She is member of the Academic Management Board of the master program of the Leading International Vaccinology Education of Erasmus/European Union and of the Ethics Committee for Research in Humans of USP.

Lenette graduated with a BA in the Honors Program with a major in Biology and minor in Asian Studies from Swarthmore College where she worked in the laboratory of Elizabeth Vallen on yeast cell cycle regulation. As part of the Medical Scientist Training Program at Case Western Reserve University, she obtained an MD and PhD in the Molecular Virology Program. Her graduate work in the laboratory of Ganes Sen focused on dsRNA mediated signaling and innate immunity in the context of paramyxovirus infections. She completed an internship and residency in Internal Medicine at New York Presbyterian – Weill Cornell and a fellowship in Infectious Diseases in the Partners program at Massachusetts General Hospital and Brigham and Women’s Hospital. Her postdoctoral research in the laboratories of Sarah Fortune at the Harvard T.H. Chan School of Public Health and Galit Alter at the Ragon Institute of MGH, MIT, and Harvard focused on delineating the humoral landscape of immune responses to Mycobacterium tuberculosis. Lenette’s initial work characterized divergent humoral profiles in patients with clinically characterized distinct tuberculosis (TB) disease states that support an immunomodulatory role for antibodies. Using this approach, she went on to examine a population of individuals highly exposed to Mtb yet clinically not recognized as part of the spectrum of human disease. She showed robust humoral profiles in the context of non-canonical T cell responses, providing immunological parameters to help define an additional state of human TB and an alternative model towards understanding host responses to Mtb exposure. Lenette joined the Division of Infectious Diseases and Geographic Medicine at UT Southwestern in 2019 with a clinical practice primarily at Parkland Health and Hospitals System and a research lab aimed at identifying the mechanisms by which antibodies modulate the host immune response in TB. Beyond TB, dissecting antibody functions is fundamentally relevant to all infectious disease where antibodies interface host and microbe, informing diagnostic, therapeutic and vaccine design.
Lenette graduated with a BA in the Honors Program with a major in Biology and minor in Asian Studies from Swarthmore College where she worked in the laboratory of Elizabeth Vallen on yeast cell cycle regulation. As part of the Medical Scientist Training Program at Case Western Reserve University, she obtained an MD and PhD in the Molecular Virology Program. Her graduate work in the laboratory of Ganes Sen focused on dsRNA mediated signaling and innate immunity in the context of paramyxovirus infections. She completed an internship and residency in Internal Medicine at New York Presbyterian – Weill Cornell and a fellowship in Infectious Diseases in the Partners program at Massachusetts General Hospital and Brigham and Women’s Hospital. Her postdoctoral research in the laboratories of Sarah Fortune at the Harvard T.H. Chan School of Public Health and Galit Alter at the Ragon Institute of MGH, MIT, and Harvard focused on delineating the humoral landscape of immune responses to Mycobacterium tuberculosis. Lenette’s initial work characterized divergent humoral profiles in patients with clinically characterized distinct tuberculosis (TB) disease states that support an immunomodulatory role for antibodies. Using this approach, she went on to examine a population of individuals highly exposed to Mtb yet clinically not recognized as part of the spectrum of human disease. She showed robust humoral profiles in the context of non-canonical T cell responses, providing immunological parameters to help define an additional state of human TB and an alternative model towards understanding host responses to Mtb exposure. Lenette joined the Division of Infectious Diseases and Geographic Medicine at UT Southwestern in 2019 with a clinical practice primarily at Parkland Health and Hospitals System and a research lab aimed at identifying the mechanisms by which antibodies modulate the host immune response in TB. Beyond TB, dissecting antibody functions is fundamentally relevant to all infectious disease where antibodies interface host and microbe, informing diagnostic, therapeutic and vaccine design.

Nicole Lurie, M.D., M.S.P.H. is currently the Strategic Advisor to the CEO and response lead at the Coalition for Epidemic Preparedness Innovations (CEPI). She is also a Senior Lecturer at Harvard Medical School, a member of the research faculty at Massachusetts General Hospital and Professor of Medicine at George Washington University School of Medicine. She served an 8-year term as Assistant Secretary for Preparedness and Response at the US Department of Health and Human Services. In that role she led the HHS response to numerous public health emergencies, ranging from infectious disease to natural and man-made disasters and is responsible for many innovations in emergency preparedness and response. She also chaired the Public Health Emergency Medical Countermeasures Enterprise, a government wide organization ultimately responsible for the development of medical countermeasures, including vaccines against pandemics and emerging threats. Dr. Lurie has a long history in health services research. Prior to federal service, she was the Paul O’Neill Professor of Policy Analysis at RAND, where she started and led the public health preparedness program and RAND’s Center for Population Health and Health Disparities. She has had leadership roles in academia, as Professor of Medicine and Public Health at the University of Minnesota, as Medical Advisor to the Commissioner, Minnesota Department of Health, and as Principal Deputy Assistant Secretary for Health at the US Department of Health and Human Services. Dr. Lurie received her BA and MD degrees from the University of Pennsylvania, and completed her residency and public health training at UCLA. Her research has focused on access to and quality of care, health system redesign, equity, mental health, public health and preparedness. She is recipient of numerous awards and is a member of the National Academy of Medicine. She continues to practice clinical medicine in a community clinic in Washington DC.
Nicole Lurie, M.D., M.S.P.H. is currently the Strategic Advisor to the CEO and response lead at the Coalition for Epidemic Preparedness Innovations (CEPI). She is also a Senior Lecturer at Harvard Medical School, a member of the research faculty at Massachusetts General Hospital and Professor of Medicine at George Washington University School of Medicine. She served an 8-year term as Assistant Secretary for Preparedness and Response at the US Department of Health and Human Services. In that role she led the HHS response to numerous public health emergencies, ranging from infectious disease to natural and man-made disasters and is responsible for many innovations in emergency preparedness and response. She also chaired the Public Health Emergency Medical Countermeasures Enterprise, a government wide organization ultimately responsible for the development of medical countermeasures, including vaccines against pandemics and emerging threats. Dr. Lurie has a long history in health services research. Prior to federal service, she was the Paul O’Neill Professor of Policy Analysis at RAND, where she started and led the public health preparedness program and RAND’s Center for Population Health and Health Disparities. She has had leadership roles in academia, as Professor of Medicine and Public Health at the University of Minnesota, as Medical Advisor to the Commissioner, Minnesota Department of Health, and as Principal Deputy Assistant Secretary for Health at the US Department of Health and Human Services. Dr. Lurie received her BA and MD degrees from the University of Pennsylvania, and completed her residency and public health training at UCLA. Her research has focused on access to and quality of care, health system redesign, equity, mental health, public health and preparedness. She is recipient of numerous awards and is a member of the National Academy of Medicine. She continues to practice clinical medicine in a community clinic in Washington DC.

Prof Hassan Mahomed, MBChB, MMed, PhD, works currently as a Public Health Medicine specialist at the Western Cape Government Dept of Health and Division of Health Systems and Public Health in the Department of Global Health at Stellenbosch University. In the Department of Health, he provides technical support for planning, monitoring and evaluation, health systems reform, health information systems development and outbreak response. He has played a key role in co-ordinating the province’s response to the COVID-19 epidemic including the vaccine rollout. At Stellenbosch University, he teaches public health and runs a clinical trials module. He supervises both masters and PhD students.
Prof Hassan Mahomed, MBChB, MMed, PhD, works currently as a Public Health Medicine specialist at the Western Cape Government Dept of Health and Division of Health Systems and Public Health in the Department of Global Health at Stellenbosch University. In the Department of Health, he provides technical support for planning, monitoring and evaluation, health systems reform, health information systems development and outbreak response. He has played a key role in co-ordinating the province’s response to the COVID-19 epidemic including the vaccine rollout. At Stellenbosch University, he teaches public health and runs a clinical trials module. He supervises both masters and PhD students.

Dr. Makanga, MD, PhD, FRCP, is a clinician-scientist with 28 years of professional experience of working on health and poverty-related infectious diseases involving Africa. This includes 24 years of work experience on medical product development and clinical regulatory activities. He holds a Medical Degree from Makerere University, Uganda, a master’s degree at the University of Liverpool, and a PhD in Pharmacology & Therapeutics at the Liverpool School of Tropical Medicine, United Kingdom. He is also a Fellow of the Royal College of Physicians of Edinburgh, Scotland.
Dr Makanga is EDCTP Executive Director. Before joining EDCTP, Dr Makanga was first in clinical practice and academia, and later clinical research and research management. Moreover, he has served in various scientific and policy advisory boards for international product development, philanthropic organisations, World Bank, European Union initiatives and pharmaceutical companies involved in developing medicinal products for poverty related and neglected diseases.
Dr. Makanga, MD, PhD, FRCP, is a clinician-scientist with 28 years of professional experience of working on health and poverty-related infectious diseases involving Africa. This includes 24 years of work experience on medical product development and clinical regulatory activities. He holds a Medical Degree from Makerere University, Uganda, a master’s degree at the University of Liverpool, and a PhD in Pharmacology & Therapeutics at the Liverpool School of Tropical Medicine, United Kingdom. He is also a Fellow of the Royal College of Physicians of Edinburgh, Scotland.
Dr Makanga is EDCTP Executive Director. Before joining EDCTP, Dr Makanga was first in clinical practice and academia, and later clinical research and research management. Moreover, he has served in various scientific and policy advisory boards for international product development, philanthropic organisations, World Bank, European Union initiatives and pharmaceutical companies involved in developing medicinal products for poverty related and neglected diseases.

Agustin Martin is an advocacy officer at DSW, following health, research and budgetary affairs. He is responsible for building relations with EU and African authorities and stakeholders, conducting legislative analysis and developing advocacy campaigns. Agustin has eight years of professional experience in EU affairs and holds Master degrees in political science and law.
Agustin Martin is an advocacy officer at DSW, following health, research and budgetary affairs. He is responsible for building relations with EU and African authorities and stakeholders, conducting legislative analysis and developing advocacy campaigns. Agustin has eight years of professional experience in EU affairs and holds Master degrees in political science and law.

Helen McShane is currently Director of the Oxford NIHR Biomedical Research Centre; Professor of Vaccinology at Oxford University; Deputy Head (Translation and Personnel), Medical Sciences Division; and an Honorary Consultant Physician in Infectious Diseases. Helen obtained an intercalated BSc in 1988, followed by a degree in medicine in 1991 (both University of London). In 1997 She was awarded an MRC Clinical Training Fellowship to undertake a PhD with Adrian Hill in Oxford, and was later awarded a PhD in 2001 (University of London). In 2001 she was awarded a Wellcome Clinician Scientist Fellowship, allowing her to complete her clinical training and subsequently awarded a CCST in HIV and GU Medicine in 2003. In 2005 and 2010, she was awarded a Wellcome Senior Clinical Research Fellowship. She currently holds a Wellcome Trust Investigator Award. Helen was elected to be a Fellow of the Academy of Medical Sciences in 2019. Since 2001, Helen has lead a TB vaccine research group at the University of Oxford. She led the development of MVA85A, the first new TB vaccine candidate to enter efficacy testing. Current areas of focus include the development of controlled human mycobacterial challenge models, aerosol delivery of vaccines and immunomonitoring in clinical trials. She collaborates with several research groups across Africa in TB vaccine clinical trials. Most recently, Helen has been leading the coordination of COVID-19 drug trials within Oxford and nationally and is now leading a programme to establish a controlled human infection model with SARS CoV2 which will allow the evaluation of protective immunity.
Helen McShane is currently Director of the Oxford NIHR Biomedical Research Centre; Professor of Vaccinology at Oxford University; Deputy Head (Translation and Personnel), Medical Sciences Division; and an Honorary Consultant Physician in Infectious Diseases. Helen obtained an intercalated BSc in 1988, followed by a degree in medicine in 1991 (both University of London). In 1997 She was awarded an MRC Clinical Training Fellowship to undertake a PhD with Adrian Hill in Oxford, and was later awarded a PhD in 2001 (University of London). In 2001 she was awarded a Wellcome Clinician Scientist Fellowship, allowing her to complete her clinical training and subsequently awarded a CCST in HIV and GU Medicine in 2003. In 2005 and 2010, she was awarded a Wellcome Senior Clinical Research Fellowship. She currently holds a Wellcome Trust Investigator Award. Helen was elected to be a Fellow of the Academy of Medical Sciences in 2019. Since 2001, Helen has lead a TB vaccine research group at the University of Oxford. She led the development of MVA85A, the first new TB vaccine candidate to enter efficacy testing. Current areas of focus include the development of controlled human mycobacterial challenge models, aerosol delivery of vaccines and immunomonitoring in clinical trials. She collaborates with several research groups across Africa in TB vaccine clinical trials. Most recently, Helen has been leading the coordination of COVID-19 drug trials within Oxford and nationally and is now leading a programme to establish a controlled human infection model with SARS CoV2 which will allow the evaluation of protective immunity.

Cheleka Anne-Marie Mpande is an immunologist by training with a passion for public engagement and science communication. Cheleka recently submitted her doctoral thesis in the field of immunology undertaken via the South African Tuberculosis Vaccine Initiative, University of Cape Town. During her graduate studies, Cheleka became involved in Eh!woza, first as a “Labbie” facilitator then as the main facilitator of the Tuberculosis Vaccinology workshops (2016-2019). In late 2020, Cheleka officially joined the Eh!woza team as the Impact Assessment Researcher, and coordinator of the scientific communications arm of Eh!woza. Her role primarily focuses on the development and implementation of innovative methods to assess the impact of Eh!woza’s public engagement projects.
Cheleka Anne-Marie Mpande is an immunologist by training with a passion for public engagement and science communication. Cheleka recently submitted her doctoral thesis in the field of immunology undertaken via the South African Tuberculosis Vaccine Initiative, University of Cape Town. During her graduate studies, Cheleka became involved in Eh!woza, first as a “Labbie” facilitator then as the main facilitator of the Tuberculosis Vaccinology workshops (2016-2019). In late 2020, Cheleka officially joined the Eh!woza team as the Impact Assessment Researcher, and coordinator of the scientific communications arm of Eh!woza. Her role primarily focuses on the development and implementation of innovative methods to assess the impact of Eh!woza’s public engagement projects.

Valerie Oriol Mathieu is Global Medical Affairs Leader, Vaccines. In her role, Valerie is the Medical Affairs Lead for the licensed Janssen vaccines and the vaccine portfolio in R&D. Valerie is a Medical Doctor, holds a Masters in strategic management, and Vaccinology degrees. After a few years of clinical practice, she worked for contract research organizations, focusing on late clinical development and post-marketing studies. In 2006, Valerie joined the vaccine industry within Medical Affairs where she worked in the field of enteric diseases, influenza and travel vaccines. She later moved to Scientific Affairs, and finally she evolved to Policy responsibilities.
For more than 5 years, Valerie has worked with Janssen Vaccines as Director Global Vaccines Policy and Partnership where she was responsible for policy strategy for candidate vaccines in development at Janssen in the field of respiratory diseases, HIV, Ebola and Extra-intestinal E.coli. In her role she has been analyzing global societal and political perspectives on public health, related to the prevention of infectious diseases through vaccination. She has developed Janssen positions on vaccine policies in order to serve Janssen reputational and business objectives. She led Janssen representation in several vaccine working groups with trade associations, public health authorities, international coalitions and expert groups. She is a founding member of VaccinesToday.eu, with expertise in knowledge sharing from high level vaccinology education to social media conversation with lay public.
In 2016, she became Global Medical Affairs Leader for Vaccines, responsible for optimizing development and use of our vaccines through qualitative and compliant engagement with medical community. She leads disseminating science, understanding medical needs, contributing to clinical development plans for late phases and post-licensure evaluation (health outcomes, real world data), preparing for vaccine program implementation in countries with a focus on platform technologies, emerging diseases and HIV. She is part of the Good Participatory Practices team, and involved in public-private interactions for development and access projects (e.g. IMI projects).
Valerie Oriol Mathieu is Global Medical Affairs Leader, Vaccines. In her role, Valerie is the Medical Affairs Lead for the licensed Janssen vaccines and the vaccine portfolio in R&D. Valerie is a Medical Doctor, holds a Masters in strategic management, and Vaccinology degrees. After a few years of clinical practice, she worked for contract research organizations, focusing on late clinical development and post-marketing studies. In 2006, Valerie joined the vaccine industry within Medical Affairs where she worked in the field of enteric diseases, influenza and travel vaccines. She later moved to Scientific Affairs, and finally she evolved to Policy responsibilities.
For more than 5 years, Valerie has worked with Janssen Vaccines as Director Global Vaccines Policy and Partnership where she was responsible for policy strategy for candidate vaccines in development at Janssen in the field of respiratory diseases, HIV, Ebola and Extra-intestinal E.coli. In her role she has been analyzing global societal and political perspectives on public health, related to the prevention of infectious diseases through vaccination. She has developed Janssen positions on vaccine policies in order to serve Janssen reputational and business objectives. She led Janssen representation in several vaccine working groups with trade associations, public health authorities, international coalitions and expert groups. She is a founding member of VaccinesToday.eu, with expertise in knowledge sharing from high level vaccinology education to social media conversation with lay public.
In 2016, she became Global Medical Affairs Leader for Vaccines, responsible for optimizing development and use of our vaccines through qualitative and compliant engagement with medical community. She leads disseminating science, understanding medical needs, contributing to clinical development plans for late phases and post-licensure evaluation (health outcomes, real world data), preparing for vaccine program implementation in countries with a focus on platform technologies, emerging diseases and HIV. She is part of the Good Participatory Practices team, and involved in public-private interactions for development and access projects (e.g. IMI projects).

Uvi Naidoo is a specialist paediatrician in Cape Town, South Africa with academic interest in childhood TB immunology. His passion as a clinician, scientist and TB advocate stems from him requiring 3years of treatment to be cured from MDR-TB. He is presently oxygen-dependent at the moment, recovering from COVID-19 complications but remains hopeful that momentum for TB eradication will not be blunted.
Uvi Naidoo is a specialist paediatrician in Cape Town, South Africa with academic interest in childhood TB immunology. His passion as a clinician, scientist and TB advocate stems from him requiring 3years of treatment to be cured from MDR-TB. He is presently oxygen-dependent at the moment, recovering from COVID-19 complications but remains hopeful that momentum for TB eradication will not be blunted.

Deepali is Senior Manager, Policy at Gavi. Her work includes the design of Gavi’s funding model and the identification of of high value vaccine investments. In her 6 years at Gavi, Deepali developed Gavi’s market-shaping strategy for 2016-2020 and co-led the Vaccine Investment Strategy in 2018. She currently oversees a portfolio of work that includes monitoring the future pipeline of vaccines of high public health priority to Gavi implementing countries. Prior to Gavi, she worked at the National Academies of Medicine in the US and was a Fulbright Scholar in Mongolia. She has an MPH from Johns Hopkins School of Public Health and a BS from Georgetown University.
Deepali is Senior Manager, Policy at Gavi. Her work includes the design of Gavi’s funding model and the identification of of high value vaccine investments. In her 6 years at Gavi, Deepali developed Gavi’s market-shaping strategy for 2016-2020 and co-led the Vaccine Investment Strategy in 2018. She currently oversees a portfolio of work that includes monitoring the future pipeline of vaccines of high public health priority to Gavi implementing countries. Prior to Gavi, she worked at the National Academies of Medicine in the US and was a Fulbright Scholar in Mongolia. She has an MPH from Johns Hopkins School of Public Health and a BS from Georgetown University.

Professor Helen Rees is Founder and Executive Director of Wits RHI at the University of Witwatersrand in Johannesburg, South Africa. She is a Personal Professor in the University of Witwatersrand’s Department of Obstetrics and Gynaecology and the Co-Director of ALIVE (African Leadership in Vaccinology Expertise) which is Wits University’s flagship vaccinology programme. She is an Honorary Professor in the Department of Clinical Research at the London School of Hygiene and Tropical Medicine (LSHTM). Prof Rees has extensive experience in the field of medicines regulation and Chairs the South African Health Products Regulatory Authority (SAHPRA). She has been very involved in national, regional and global response efforts to COVID-19 including the development of COVID-19 vaccines, their potential rollout and utilization. In South Africa, Prof Rees is a member of the Ministerial Advisory Committee on COVID-19, a member of the Ministerial Advisory Committee on COVID-19 vaccines and Chairs the VACC-MAC COVID-19 Variant Technical Working Group. Internationally, she is a member of the COVAX committee on COVID-19 maternal immunization, a member of WHO’s expert committee on COVID-19 vaccines and a member of WHO’s Scientific and Technical Advisory Group on Infectious Hazards. GAVI, CEPI and WHO are jointly driving the global COVID vaccine effort including the COVAX facility, and Prof Rees is involved with the oversight of the COVAX facility. She is a member of the WHO IHR Emergency Committee on COVID-19. Prof Rees has worked extensively with WHO and other institutions in the African region and Chairs the WHO’s African Regional Immunisation Technical Advisory Group on Immunization (RITAG). Prof Rees is widely recognised for her work as a global health practitioner and has been appointed as chair and member of many international scientific committees and Boards. She is currently the chair of WHO’s International Health Regulation (IHR) Polio Emergency Committee and Co-Chair of the WHO SAGE Working Group on Ebola Vaccines. Prof Rees is a member of the Global Alliance for Vaccines and Immunization (Gavi) Board and chairs the Gavi Programme and Policy Committee. She is a member of the Coalition for Epidemic Preparedness and Innovation (CEPI) Board and chairs the CEPI Scientific Advisory Committee.
Professor Helen Rees is Founder and Executive Director of Wits RHI at the University of Witwatersrand in Johannesburg, South Africa. She is a Personal Professor in the University of Witwatersrand’s Department of Obstetrics and Gynaecology and the Co-Director of ALIVE (African Leadership in Vaccinology Expertise) which is Wits University’s flagship vaccinology programme. She is an Honorary Professor in the Department of Clinical Research at the London School of Hygiene and Tropical Medicine (LSHTM). Prof Rees has extensive experience in the field of medicines regulation and Chairs the South African Health Products Regulatory Authority (SAHPRA). She has been very involved in national, regional and global response efforts to COVID-19 including the development of COVID-19 vaccines, their potential rollout and utilization. In South Africa, Prof Rees is a member of the Ministerial Advisory Committee on COVID-19, a member of the Ministerial Advisory Committee on COVID-19 vaccines and Chairs the VACC-MAC COVID-19 Variant Technical Working Group. Internationally, she is a member of the COVAX committee on COVID-19 maternal immunization, a member of WHO’s expert committee on COVID-19 vaccines and a member of WHO’s Scientific and Technical Advisory Group on Infectious Hazards. GAVI, CEPI and WHO are jointly driving the global COVID vaccine effort including the COVAX facility, and Prof Rees is involved with the oversight of the COVAX facility. She is a member of the WHO IHR Emergency Committee on COVID-19. Prof Rees has worked extensively with WHO and other institutions in the African region and Chairs the WHO’s African Regional Immunisation Technical Advisory Group on Immunization (RITAG). Prof Rees is widely recognised for her work as a global health practitioner and has been appointed as chair and member of many international scientific committees and Boards. She is currently the chair of WHO’s International Health Regulation (IHR) Polio Emergency Committee and Co-Chair of the WHO SAGE Working Group on Ebola Vaccines. Prof Rees is a member of the Global Alliance for Vaccines and Immunization (Gavi) Board and chairs the Gavi Programme and Policy Committee. She is a member of the Coalition for Epidemic Preparedness and Innovation (CEPI) Board and chairs the CEPI Scientific Advisory Committee.

Alex Schmidt is Head of Vaccine Development at the Bill & Melinda Gates Medical Research Institute. Alex received his M.D./Ph.D. from Freie Universität Berlin and trained in pediatrics at Charité and The German Heart Center. He completed his postdoctoral training in the Laboratory of Infectious Diseases (LID) at NIAID, NIH, and then returned to Berlin for group leader & faculty positions in pediatrics. He re-joined LID from 2005 to 2011 for translational and clinical R&D, and then joined GSK Vaccines, where he led clinical vaccine development programs for dengue, RSV and influenza viruses. Alex joined Gates MRI in 2018 as the clinical lead for TB vaccine development.
Alex Schmidt is Head of Vaccine Development at the Bill & Melinda Gates Medical Research Institute. Alex received his M.D./Ph.D. from Freie Universität Berlin and trained in pediatrics at Charité and The German Heart Center. He completed his postdoctoral training in the Laboratory of Infectious Diseases (LID) at NIAID, NIH, and then returned to Berlin for group leader & faculty positions in pediatrics. He re-joined LID from 2005 to 2011 for translational and clinical R&D, and then joined GSK Vaccines, where he led clinical vaccine development programs for dengue, RSV and influenza viruses. Alex joined Gates MRI in 2018 as the clinical lead for TB vaccine development.

Dr. Cherise P. Scott is a global health specialist with over a decade of experience in developing and advancing innovations and products for neglected diseases. Dr. Scott’s experience spans preclinical to market work, and she has collaborated with stakeholders and partners in resource-limited settings across 30 countries. She received her PhD in international health with a focus on tuberculosis and vaccine development from Johns Hopkins Bloomberg School of Public Health. She has a Master of Public Health and a BS in biology from Florida A & M University.
Dr. Cherise P. Scott is a global health specialist with over a decade of experience in developing and advancing innovations and products for neglected diseases. Dr. Scott’s experience spans preclinical to market work, and she has collaborated with stakeholders and partners in resource-limited settings across 30 countries. She received her PhD in international health with a focus on tuberculosis and vaccine development from Johns Hopkins Bloomberg School of Public Health. She has a Master of Public Health and a BS in biology from Florida A & M University.

Dr. Manjula Singh, is Scientist E (Deputy Director General), Division of Epidemiology and Communicable Diseases, at Indian Council of Medical Research (ICMR), New Delhi, India. She is a Medical Doctor with Ph.D in ‘Immunology’ and training in Dermatology, Venereology and Leprology.
She has a vast experience of more than 18 years in the area of Tuberculosis, leprosy & HIV research and has been involved in many clinical trials in these areas. Currently she is the Programme Officer for tuberculosis research at ICMR including Indo-US collaboration on tuberculosis research and is the co-ordinator of several clinical and implementation research studies on TB.
She is a member of National Technical Resource Group of National TB Elimination Programme (NTEP), Central TB Division under Ministry of Health & family Welfare, Government of India and has also served as member of WHO’s Global Task Force on TB Research. She is the coordinator of TB research activities of the ‘BRICS TB research network’ from ICMR and is involved in planning and executing multicountry research activities among BRICS countries.
She is the key person involved in the establishment and co-ordination of activities under ‘India TB Research consortium’ (ITRC), a flagship programme of ICMR focussed on development of new tools and strategies in four thematic areas (diagnostics, therapeutics, vaccines and implementation research) of TB research to tackle TB in a mission mode which has won the prestigious International ‘KOCHON Prize’ 2017 for accelerating TB R&D in the country. She is co-ordinating several studies on newer drug regimen, newer diagnostics and implementation strategies under ITRC. She is currently leading the Phase III TB vaccine trial with two vaccines for prevention of TB in healthy household contacts of TB cases.
She has won the ‘BMJ infectious disease initiative of the year in 2018’ and National e-Governance award, 2019 by Ministry of Public Reforms & Public Grievances, Government of India for ‘Outstanding research on citizen centric services’ by research Institutions for undertaking the multicentric research of mobile TB diagnostics van intervention in tribal areas in 5 states of India through ICMR Institutes.
Dr. Manjula Singh, is Scientist E (Deputy Director General), Division of Epidemiology and Communicable Diseases, at Indian Council of Medical Research (ICMR), New Delhi, India. She is a Medical Doctor with Ph.D in ‘Immunology’ and training in Dermatology, Venereology and Leprology.
She has a vast experience of more than 18 years in the area of Tuberculosis, leprosy & HIV research and has been involved in many clinical trials in these areas. Currently she is the Programme Officer for tuberculosis research at ICMR including Indo-US collaboration on tuberculosis research and is the co-ordinator of several clinical and implementation research studies on TB.
She is a member of National Technical Resource Group of National TB Elimination Programme (NTEP), Central TB Division under Ministry of Health & family Welfare, Government of India and has also served as member of WHO’s Global Task Force on TB Research. She is the coordinator of TB research activities of the ‘BRICS TB research network’ from ICMR and is involved in planning and executing multicountry research activities among BRICS countries.
She is the key person involved in the establishment and co-ordination of activities under ‘India TB Research consortium’ (ITRC), a flagship programme of ICMR focussed on development of new tools and strategies in four thematic areas (diagnostics, therapeutics, vaccines and implementation research) of TB research to tackle TB in a mission mode which has won the prestigious International ‘KOCHON Prize’ 2017 for accelerating TB R&D in the country. She is co-ordinating several studies on newer drug regimen, newer diagnostics and implementation strategies under ITRC. She is currently leading the Phase III TB vaccine trial with two vaccines for prevention of TB in healthy household contacts of TB cases.
She has won the ‘BMJ infectious disease initiative of the year in 2018’ and National e-Governance award, 2019 by Ministry of Public Reforms & Public Grievances, Government of India for ‘Outstanding research on citizen centric services’ by research Institutions for undertaking the multicentric research of mobile TB diagnostics van intervention in tribal areas in 5 states of India through ICMR Institutes.

Dr Soumya Swaminathan was appointed WHO’s first Chief Scientist in March 2019. A paediatrician from India and a globally recognized researcher on tuberculosis and HIV, she brings with her 30 years of experience in clinical care and research and has worked throughout her career to translate research into impactful programmes. Dr Swaminathan was Secretary to the Government of India for Health Research and Director General of the Indian Council of Medical Research from 2015 to 2017. In that position, she focused on bringing science and evidence into health policy making, building research capacity in Indian medical schools and forging south-south partnerships in health sciences. From 2009 to 2011, she also served as Coordinator of the UNICEF/UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases in Geneva.
She received her academic training in India, the United Kingdom, and the United States of America, and has published more than 350 peer-reviewed publications and book chapters. She is an elected Foreign Fellow of the US National Academy of Medicine and a Fellow of all three science academies in India. The Science division’s role is to ensure that WHO stays ahead of the curve and leverages advances in science and technology for public health and clinical care, as well as ensuring that the norms, standards and guidelines produced by WHO are scientifically excellent, relevant and timely. Her vision is to ensure that WHO is at the cutting edge of science and is able to translate new knowledge into meaningful impact on population health worldwide.
Dr Soumya Swaminathan was appointed WHO’s first Chief Scientist in March 2019. A paediatrician from India and a globally recognized researcher on tuberculosis and HIV, she brings with her 30 years of experience in clinical care and research and has worked throughout her career to translate research into impactful programmes. Dr Swaminathan was Secretary to the Government of India for Health Research and Director General of the Indian Council of Medical Research from 2015 to 2017. In that position, she focused on bringing science and evidence into health policy making, building research capacity in Indian medical schools and forging south-south partnerships in health sciences. From 2009 to 2011, she also served as Coordinator of the UNICEF/UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases in Geneva.
She received her academic training in India, the United Kingdom, and the United States of America, and has published more than 350 peer-reviewed publications and book chapters. She is an elected Foreign Fellow of the US National Academy of Medicine and a Fellow of all three science academies in India. The Science division’s role is to ensure that WHO stays ahead of the curve and leverages advances in science and technology for public health and clinical care, as well as ensuring that the norms, standards and guidelines produced by WHO are scientifically excellent, relevant and timely. Her vision is to ensure that WHO is at the cutting edge of science and is able to translate new knowledge into meaningful impact on population health worldwide.

C. Fordham von Reyn (“Ford”) MD, DSc (Hon) is Professor of Medicine, Infectious Disease and International Health, and Director, DarDar International Programs at Geisel School of Medicine at Dartmouth. He is a cum laude graduate of Harvard Medical School where he also completed a Fellowship in Infectious Disease. He served with the Centers for Disease Control and subsequently as a founding staff member for the Special Program on AIDS of the World Health Organization. His research has focused on the international epidemiology of mycobacterial infections in HIV and development of an inactivated whole cell TB vaccine. He was PI for the 7-year NIH-sponsored Phase 3 trial of SRL172 which remains the only vaccine shown effective in preventing TB disease. He is currently focused on the development of DAR-901 which represents a scalable manufacturing process for SRL172. A Phase 1 trial of DAR-901 was completed in the US and a Phase 2b trial recently completed in Dar-es-Salaam. He continues his long term Fogarty training grant collaboration with colleagues in Tanzania.
C. Fordham von Reyn (“Ford”) MD, DSc (Hon) is Professor of Medicine, Infectious Disease and International Health, and Director, DarDar International Programs at Geisel School of Medicine at Dartmouth. He is a cum laude graduate of Harvard Medical School where he also completed a Fellowship in Infectious Disease. He served with the Centers for Disease Control and subsequently as a founding staff member for the Special Program on AIDS of the World Health Organization. His research has focused on the international epidemiology of mycobacterial infections in HIV and development of an inactivated whole cell TB vaccine. He was PI for the 7-year NIH-sponsored Phase 3 trial of SRL172 which remains the only vaccine shown effective in preventing TB disease. He is currently focused on the development of DAR-901 which represents a scalable manufacturing process for SRL172. A Phase 1 trial of DAR-901 was completed in the US and a Phase 2b trial recently completed in Dar-es-Salaam. He continues his long term Fogarty training grant collaboration with colleagues in Tanzania.

Richard G White (BSc, MSc, PhD) is Professor of Infectious Disease Modelling in the Centre for the Mathematical Modelling of Infectious Diseases and the TB Centre at the London School of Hygiene and Tropical Medicine. He is Director of the TB Modelling and Analysis Consortium and leads the LSHTM TB Modelling Group. Richard’s research focus is the mathematical and statistical modelling of the transmission and control of infectious diseases, particularly TB and HIV. He has a strong focus on the use of modelling to accelerate the development and deployment of TB vaccines.
Richard G White (BSc, MSc, PhD) is Professor of Infectious Disease Modelling in the Centre for the Mathematical Modelling of Infectious Diseases and the TB Centre at the London School of Hygiene and Tropical Medicine. He is Director of the TB Modelling and Analysis Consortium and leads the LSHTM TB Modelling Group. Richard’s research focus is the mathematical and statistical modelling of the transmission and control of infectious diseases, particularly TB and HIV. He has a strong focus on the use of modelling to accelerate the development and deployment of TB vaccines.