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Pfizer & BioNTech Receives MHRA's EUA for BNT162b2 Against COVID-19

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Pfizer & BioNTech Receives MHRA's EUA for BNT162b2 Against COVID-19

Pfizer & BioNTech Receives MHRA's EUA for BNT162b2 Against COVID-19

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  • Pfizer & BioNTech reports that the MHRA in the UK has granted a temporary authorization for the EU for BNT162b2 against COVID-19. The distribution of vaccine will be prioritized according to the populations identified in guidance from the JCVI
  • The MHRA’s decision is based on a rolling submission- including data from the P-III study- demonstrating 95% efficacy in participants without & with/ out prior SARS-CoV-2 infection- in each case measured from 7 days after the second dose
  • This marks the first EUA following a WW P-III trial of a vaccine to combat the pandemic. The companies are anticipating further regulatory decisions across the globe in Dec’2020

 ­ Ref: Pfizer | Image: The Jakarta Post

Click here to­ read the full press release 

Tuba

Tuba was Senior Editor at PharmaShots. She was curious, creative, and passionate about recent updates and innovations in the life sciences industry. She covered Biopharma, MedTech, and Digital health segments. Tuba also had an experience in digital and social media marketing and ran the campaigns independently. She can be contacted at connect@pharmashots.com.

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