CDRH Wants To Check Out Manufacturing Facilities
This article was originally published in The Silver Sheet
FDA’s device center wants to extend its Experiential Learning Program, wherein CDRH product review staffers visit manufacturing and clinical facilities to learn more about the devices they oversee.
You may also be interested in...
Submission surge in late 2019 means a spike in late summer 2020 user fee goals, including 16 novel agents in August alone.
Keeping Track: Approvals For Tazverik And Tepezza, Priority Reviews For Belantamab Mafodotin And Lynparza
The latest drug development news and highlights from our US FDA Performance Tracker.
Accelerated approval in epithelial sarcoma may de-risk the firm’s goals for approval of Tazverik in follicular lymphoma and other larger indications.