The US Food and Drug Administration is putting itself in a better position to check whether, and under what conditions, generic drugs it has approved remain bioequivalent to their brand counterparts by contracting for more capability to run its own clinical bioequivalence trials.
Such studies could help build trust among providers and patients in the quality of generic drug products, while also building...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Generics Bulletin 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?