The US Food and Drug Administration confirmed in a 19 August guidance document that it will generally issue complete response letters to sponsors when it has concerning information about the manufacturing facilities listed in their product marketing applications but cannot conduct a timely pre-approval inspection, or PAI, due to the pandemic.
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?