The Food and Drug Omnibus Reform Act (FDORA) gave the US FDA authority to require that confirmatory trials be underway at the time of accelerated approval. Although the legislation was signed into law just days before the start of 2023, the class of novel products that came to market under the expedited pathway last year reflects the philosophy behind that legislation.
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?