U. S. FDA/X
Apr 18, 2025, 16:45
Do you have questions about reporting requirements for medical device convenience kit manufacturers? – U.S. FDA
U.S. FDA shared on X:
” ‘Do you have questions about reporting requirements for medical device convenience kit manufacturers?
Visit our new FAQ page titled Convenience Kit Reporting Requirements for Corrections, Removals, and Recalls, or Adverse Events to learn about your responsibilities.’ ”
More posts featuring U.S. FDA on OncoDaily.
-
Challenging the Status Quo in Colorectal Cancer 2024
December 6-8, 2024
-
ESMO 2024 Congress
September 13-17, 2024
-
ASCO Annual Meeting
May 30 - June 4, 2024
-
Yvonne Award 2024
May 31, 2024
-
OncoThon 2024, Online
Feb. 15, 2024
-
Global Summit on War & Cancer 2023, Online
Dec. 14-16, 2023
May 11, 2025, 11:17
May 11, 2025, 11:17
May 11, 2025, 11:10
May 11, 2025, 11:04
May 11, 2025, 10:47
May 11, 2025, 10:32
May 11, 2025, 10:23