The US Food and Drug Administration would be prohibited from reviewing or approving a drug or biologic application submitted “by a sponsor located in Russia,” unless the application is for a drug intended to treat a serious or life-threatening condition and for which there is an unmet medical treatment need, per an amendment tacked on to the House Committee on Appropriations fiscal year 2023 FDA fundingbill.
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?