FDA will allow up to 10 minor deficiencies before automatically refusing to receive an abbreviated new drug application under an increasingly formalized generic drug user fee submission process.
In a draft guidance on ANDA refuse-to-receive standards issued Sept. 30, FDA said it will work with sponsors...
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?