23 April, 2021

13:00 to 14:15UTC+02:00

BIOTECH, DEVELOPING AND DEVELOPED COUNTRIES VACCINE MANUFACTURERS COVID-19 PRESS BRIEFING (23 April 2021)

BIOTECH, DEVELOPING AND DEVELOPED COUNTRIES VACCINE MANUFACTURERS COVID-19 PRESS BRIEFING (23 April 2021)

Online Event

Challenges and solutions to scaling up COVID-19 vaccine manufacturing capacity

When: Friday, 23 April 2021, 13:00 PM – 14:15 PM CET – Geneva / 07:00 AM –08:15 AM EDT – New York

The Biotechnology Innovation Organization (BIO), Developing Countries Vaccine Manufacturers Network (DCVMN) and the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA) are all COVID-19 vaccine manufacturers partners of COVAX.  The media briefing, hosted by IFPMA, will take stock of the contribution and difficulties of scaling up COVID-19 vaccines production, and the short and longer term challenges that need to be addressed to achieve equitable access to vaccines against COVID-19 pandemic.

For any questions, please contact: communications@ifpma.org

13:00

Speakers:

  • Roger Connor, President, Global Vaccines, GlaxoSmithKline & Vaccines CEO representative on COVAX
  • Stéphane Bancel, Chief Executive Officer, Moderna
  • Sai Prasad, Executive Director, Quality Operations, Bharat Biotech, President, Developing Countries Vaccine Manufacturers’ Network (DCVMN)
  • Rajinder Suri, Chief Executive Officer, Developing Countries Vaccine Manufacturers’ Network (DCVMN)
  • Dr. Michelle McMurry-Heath, President & CEO, Biotechnology Innovation Organization (BIO)
  • Thomas Cueni, Director General, International Federation of Pharmaceutical Manufacturers & Associations (IFPMA)

Roger Connor

Roger Connor

President, Global Vaccines, GlaxoSmithKline & Vaccines CEO representative on COVAX

Since 2018, Roger Connor has been leading GSK’s Vaccine business, comprising more than 16,000 employees worldwide working to deliver around 2 million doses every day to help protect people throughout their lives all around the globe. The business has a portfolio of more than 30 vaccines, a pipeline of 18 candidate vaccines in development and a turnover of £7.2 billion in 2019. Roger is also responsible for GSK’s global procurement organisation.
Roger chairs the Vaccines CEO group within the global trade body IFPMA and is the industry representative to the Gavi Board. He also represents the industry in the COVAX Facility, which is the organisation tasked with delivering global access for COVID-19 vaccines.
Roger was previously President of Global Manufacturing & Supply for the pharmaceuticals and consumer healthcare businesses. Prior to this, he was Vice President, Office of the CEO and Corporate Strategy. In this role, he served as secretary to the CET, as well as having responsibility for developing the GSK long-range financial forecast, related analyses and benchmarking, and integrating the key transformation initiatives.
Roger joined GSK in 1998 from AstraZeneca and has worked in a number of roles within finance and manufacturing.
He holds a Degree in Mechanical and Manufacturing Engineering from Queen’s University Belfast and a Masters in Manufacturing Leadership from Cambridge University. He is also a qualified Chartered Accountant, having trained with PriceWaterhouseCoopers.

Sai Prasad

Sai Prasad

Executive Director, Quality Operations, Bharat Biotech, President, Developing Countries Vaccine Manufacturers’ Network (DCVMN)

Sai Prasad is the Executive Director of Quality Operations at Bharat Biotech. In his current role, he oversees all aspects of quality management including quality assurance, control, and management systems and is responsible for product development and commercialisation of vaccines and biologics. He has 25 years of experience in management, biotechnology, good manufacturing practice, operations and quality management.
Previously, Mr Prasad was the Director of Molecular Otolaryngology Research Laboratories at the University of Iowa (USA). In his previous role, as the Vice President for Business Development and Corporate Strategy at Bharat Biotech International Ltd, he handled operational and strategic activities ranging from product development, innovation to corporate expansion.
He holds a degree in Biochemistry from the University of Wisconsin (USA) and an MBA in Finance and Marketing from the University of Iowa (USA). He has written more than a dozen publications related to human genetics, cell biology, molecular biology and vaccines.

Rajinder Suri

Rajinder Suri

Chief Executive Officer, Developing Countries Vaccine Manufacturers’ Network (DCVMN)

Rajinder Kumar Suri joined Developing Countries Vaccine Manufacturers’ Network, DCVMN as CEO w.e.f. Jan 15th, 2021.
Before this he was donning the hat of Chief Executive-Biologicals, Panacea Biotec Ltd. a leading Indian Biotech Company.
Rajinder has over 40 years of rich experience in Pharmaceuticals & Biological products in India & International markets out of which over 24 years’ experience at the top management level including four years on the Board of Directors of the Indian subsidiary of Sanofi Pasteur. The remaining 19 years being with Pharma out of which 16 years with Lupin, one of top 10 Indian Pharma Companies.
Mr Suri brings with him over 3 years of consulting experience as CEO & Senior Advisor, Arete Business Advisors.
Rajinder has been Member-Policy & Planning Committee (PPC), an advisory body to GAVI Board, representing DCVMN from October 2013 till June 2017, as also a Member of GAVI Steering Committee for Supply & Procurement Strategy. He has played a lead role in negotiations & interactions with Ministry of Health, Government of India, UN agencies and other Global organizations like WHO, UNICEF, Bill & Melinda Gates Foundation, Clinton Health Access Initiative & several others.
Rajinder is a former Member Executive Committee & Vice-President, DCVMN for a period of two years from Oct.2014-Oct.2016.

Thomas Cueni

Thomas Cueni

Director General, IFPMA

Thomas B. Cueni is Director General of International Federation of Pharmaceutical Manufacturers (IFPMA), the global association of research-based pharmaceutical companies and associations. Based in Geneva, IFPMA has official relations with the United Nations and contributes industry expertise to help the global health community find solutions that improve global health. Mr. Cueni is Secretary of the Biopharmaceutical CEO Roundtable (BCR), a policy forum of the global CEOs of IFPMA member companies. He is also Chair of the Business at OECD Health Committee, and also serves on the Board of Directors of the City Cancer Challenge (CCan), an initiative aiming to improve cancer care in major cities in low- and middle-income countries. In addition, Mr. Cueni serves as Industry Co-Chair of the APEC Biopharmaceutical Working Group on Ethics and Chair of the Board of the cross-sectoral AMR Industry Alliance, a group comprising more than 100 companies and associations representing Rx pharma, generics, biotech, and diagnostics committed to tackling the threat of antimicrobial resistance.
Prior to joining IFPMA he was Secretary General of Interpharma, the association of pharmaceutical research companies in Switzerland, and for many years was a member of the Board and Chair of a key committee of the European Federation of Pharmaceutical Industries and Associations. Prior to his appointment with Interpharma, Mr. Cueni had a career as a journalist, inter alia as London correspondent for the “Basler Zeitung” and “Der Bund”, and he served as a Swiss career diplomat with postings in Paris (OECD) and Vienna (IAEA, UNIDO). Mr Cueni studied economics and politics from University of Basle, the London School of Economics, and the Geneva Graduate Institute for International Studies.

Dr. Michelle McMurry-Heath

Dr. Michelle McMurry-Heath

President & CEO, Biotechnology Innovation Organization (BIO)

Michelle McMurry-Heath assumed the leadership of the Biotechnology Innovation Organization (BIO) as President and CEO on June 1, 2020. A medical doctor and molecular immunologist by training, Dr. McMurry-Heath becomes just the third chief executive to steward the world’s largest biotechnology advocacy group since BIO’s founding in 1993.
The common thread in McMurry-Heath’s work across academia, government and industry has been her focus on broadening access to scientific progress so more patients from diverse backgrounds can benefit from cutting-edge innovation. Driven by her own past family experiences navigating clinical trials and funding uncertainties within the rare disease community, McMurry-Heath calls “the distribution of scientific progress the social justice issue of our age.”
She comes to BIO from Johnson & Johnson where she served as Global Head of Evidence Generation for Medical Device Companies and then Vice President of Global External Innovation and Global Leader for Regulatory Sciences. She was also instrumental in bringing J&J’s incubator, JLabs, to Washington, DC. She led a global team of 900 with responsibilities in 150 countries around the globe.
Prior to her time at J&J, Dr. McMurry-Heath was also a key science policy leader in government. The Obama-Biden transition team tapped her to conduct a comprehensive analysis of the National Science Foundation’s policies, programs and personnel. President Obama then named her associate science director of the FDA’s Center for Devices and Radiological Health under Commissioner Peggy Hamburg. In that role, she championed clinical trial evolution, the use of real-world evidence in product evaluation, and an embrace of the patient’s voice in health research so new medical products deliver outcomes that matter to them.
McMurry-Heath was the founding director of the Aspen Institute’s Health, Biomedical Science, and Society Policy Program, where she promoted personalized medicine and bolstered international preparation for pandemic disease threats. She received her early training in science policy from the Robert Wood Johnson Foundation and later served as Senator Joe Lieberman’s top legislative aide for science and health. In that role, she drafted legislation to protect the country from biological attacks.
McMurry-Heath received her MD/PhD from Duke’s Medical Scientist Training Program, becoming the first African-American to graduate from the prestigious program. She spent 12 years working at the research bench before taking policy and leadership roles in government and industry.

Stéphane Bancel

Stéphane Bancel

Chief Executive Officer, Moderna

Stéphane Bancel has served as Moderna's Chief Executive Officer since October 2011 and as a member of Moderna’s board of directors since March 2011. Before joining the Company, Mr. Bancel served for five years as Chief Executive Officer of the French diagnostics company bioMérieux SA. From July 2000 to March 2006, he served in various roles at Eli Lilly and Company, including as Managing Director, Belgium and as Executive Director, Global Manufacturing Strategy and Supply Chain. Prior to Lilly, Mr. Bancel served as Asia-Pacific Sales and Marketing Director for bioMérieux.
Mr. Bancel currently serves on the board of directors of Qiagen N.V. and Indigo. He is currently a Venture Partner at Flagship Pioneering and a trustee of the Museum of Science in Boston. Mr. Bancel holds a Master of Engineering degree from École Centrale Paris (ECP), a Master of Science in chemical engineering from the University of Minnesota, and an M.B.A. from Harvard Business School.

23rd Apr 2021

13:00 to 14:15 UTC+02:00

Online Event

Presentation Documents:
COVID-19 vaccine industry cautions immediate action needed  to remove manufacturing supply barriers to meet production targets and keep on course to equitable and fair access to COVID-19 vaccines
News Releases
News Releases

On the 1st anniversary of ACT-Accelerator, COVID-19 vaccine makers representing biotechnology firms, developing and developed country manufacturers renew their commitment ...

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BIO-DCVMN-IFPMA COVID-19 Press Briefing - 23 April 2021 (Video)
Videos
Videos

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