Peter Marks, director of the US Food and Drug Administration’s Center for Biologics Evaluation and Research, criticized the UK’s quick release of a safety notice on adverse events about Pfizer/BioNTech’s COVID vaccine, saying there was too little context for public understanding.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?