otc monograph reform overview of draft guidance for formal meetings
Published 2 years ago • 1.9K plays • Length 54:40Download video MP4
Download video MP3
Similar videos
-
53:25
otc monograph reform: omor format and content & electronic submissions
-
47:40
otc monograph reform: deemed final orders
-
42:44
otc monograph reform: otc sunscreen drugs
-
49:43
otc monograph reform in the cares act: safety orders
-
56:47
monograph reform is here! learn what to expect and how to prepare.
-
51:01
otc monograph drug user fee program (omufa): understanding fy 2023 user fees and registration
-
49:29
otc monograph drug user fee program (omufa): understanding fy 2021 user fees
-
4:07
what is the over-the-counter (otc) drug monograph process?
-
10:55
importing fda-regulated products: the import process
-
12:36
orange book exclusivity: an introduction and overview
-
1:48:36
reporting drug amount under section 510(j)(3) of the fd&c act – session 3 and closing remarks
-
27:10
overview of post-approval chemistry, manufacture, and controls (cmc) changes to an nda - redi 2020
-
55:40
nonprescription drug product with an additional condition for nonprescription use
-
52:54
changes to orange book patent information
-
29:03
webinar wednesday - over the counter otc drug product testing
-
18:10
sbia program overview - redi 2020
-
52:33
fda drug manufacturing inspections - redi 2020
-
1:15:17
regulatory education for industry (redi) annual conference 2023 – day 1 – session 2