USFDA 21CFR
USFDA 21CFR
- Drug product salvaging as per USFDA CFR 211.208
- Expiration dating as per USFDA CFR 211.137
- Stability testing as per USFDA CFR 211.166
- General requirements For Laboratory Controls as per USFDA CFR 211.160
- Laboratory records as per USFDA CFR 211.194
- Complaint files as per USFDA CFR 211.198
- Distribution records as per USFDA CFR 211.196
- Production record review (USFDA CFR 211.192)
- Returned drug products (USFDA CFR 211.204 )