The new head of the US Food and Drug Administration’s generic drugs office suggested their regulatory foundation, the Hatch-Waxman Act, may need some updates to handle the growing number of complex products seeking approval.
Iilun Murphy, who became director of the Office of Generic Drugs on 18 June, said in an interview with the...
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?