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BioWorld - Thursday, March 26, 2026
Home » Topics » Drugs » Vaccine

Vaccine
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U.S. Capitol building

Senator: Now’s the time to plan for next pandemic

June 10, 2020
By Mari Serebrov
Before the lessons of COVID-19 fade into yesterday’s news, Congress should start preparing for the next pandemic, Sen. Lamar Alexander (R-Tenn.) is advising. As the chair of the Senate Health, Education, Labor and Pensions Committee, the senator issued a white paper Tuesday identifying areas that must be addressed.
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Gloved hand holding COVID-19 vaccine vial, syringe

BIO Digital: COVID-19 vaccines outlook offers reasons for hope, concern

June 10, 2020
By Michael Fitzhugh
Threads of hope and caution stitched together a wide-ranging appraisal of COVID-19 vaccines at June 9's BIO Digital plenary, "A Way Forward." The good news, delivered by one of the world's most sober participants in the pandemic response, mercifully came first.
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Vaccine administration

Gavi sets up advance market commitment program for COVID-19 vaccines

June 9, 2020
By Nuala Moran
LONDON – The foundation stone of a system to ensure equitable access to COVID-19 vaccines was put in place by the global vaccines summit on June 4, with 12 donors pledging $567 million in seed money for an advance market commitment (AMC) program.
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Model of clamped vaccine antigen

CSL, University of Queensland partner with CEPI to bring COVID-19 vaccine to the clinic

June 9, 2020
By Tamra Sami
PERTH, Australia – Aussie biotech CSL Ltd. and the University of Queensland (UQ) have entered a development agreement with the Coalition for Epidemic Preparedness Innovations (CEPI) to accelerate development, manufacture and distribution of a COVID-19 vaccine candidate developed by the University of Queensland.
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European Union map and coronavirus

European Commission working on procurement plan as COVID-19 vaccine race accelerates

June 9, 2020
By Nuala Moran
LONDON – The European Commission is laying plans for joint procurement of COVID-19 vaccines on behalf of all 27 EU member states, and is in discussions to agree on a harmonized approach to access and who gets vaccinated first.
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Model of clamped vaccine antigen

CSL, University of Queensland partner with CEPI to bring COVID-19 vaccine to the clinic

June 8, 2020
By Tamra Sami
PERTH, Australia – Aussie biotech CSL Ltd. and the University of Queensland (UQ) have entered a development agreement with the Coalition for Epidemic Preparedness Innovations (CEPI) to accelerate  development, manufacture and distribution of a COVID-19 vaccine candidate developed by the University of Queensland.
Read More
Vaccine administration

Gavi sets up advance market commitment program for COVID-19 vaccines

June 5, 2020
By Nuala Moran
LONDON – The foundation stone of a system to ensure equitable access to COVID-19 vaccines was put in place by the global vaccines summit on June 4, with 12 donors pledging $567 million in seed money for an advance market commitment (AMC) program.
Read More
Glass vial production line

Supply shortages continue to threaten pandemic response

June 4, 2020
By Mari Serebrov
During a massive disaster or a pandemic, securing the necessary manufacturing capacity, needles, syringes, vials, properly labeled caps, reagents and other supplies is as critical as the development of the product itself. Some experts have been warning about these needs since COVID-19 first began spreading outside of China. Now members of Congress are sounding the alarm.
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Researcher in PPE looking at three vials

WHO launches COVID-19 patent pool, backed by 35+ countries

June 2, 2020
By Nuala Moran
LONDON – The World Health Organization (WHO) is stepping up its effort to try and ensure equitable access to any approved COVID-19 vaccines and therapies, putting in place a system for sharing all intellectual property, information and clinical trials data needed to enable generic manufacturing.
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U.S. FDA headquarters

FDA’s Hahn emphasizes regulatory flexibility, but FDA not ‘walking away’ from RCTs

June 1, 2020
By Mark McCarty
The COVID-19 pandemic has demanded much of the FDA, and commissioner Stephen Hahn said on a June 1 conference call that “there have been hiccups along the way” as the enormity of the threat came into view. The agency’s use of emergency use authorizations (EUAs) has drawn criticism, but Hahn defended those EUAs and other regulatory flexibilities even has he declared that the FDA is not “walking away from” randomized, controlled clinical trials as the gold standard for premarket review.
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