- Docket Number:
- FDA-1993-D-0128
- Issued by:
-
Guidance Issuing Office
Center for Drug Evaluation and Research
It is important to harmonize the way to gather and, if necessary, to take action on important clinical safety information arising during clinical development.
Submit Comments
You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))
If unable to submit comments online, please mail written comments to:
Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852
All written comments should be identified with this document's docket number: FDA-1993-D-0128.
