As the US Food & Drug Administration moves back to in-person advisory committees after four years of pandemic-induced virtual meetings, stakeholders are likely to see different approaches in how the panels are utilized by the drug and biologics product centers and the Oncology Center of Excellence.
While there is agreement on some big-picture issues – such as the need to return to in-person meetings – 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?