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  1. Regulatory Information

GUIDANCE DOCUMENT

IOM Index March 2019

Final

This guidance is being distributed for comment purposes only.

IOM Index

Submit Comments by 03/01/2020

Although you can comment on any guidance at any time (see 21 CFR 10.115(g)(5)), to ensure that the FDA considers your comment on a draft guidance before it begins work on the final version of the guidance, submit either online or written comments on the draft guidance before the close date.

If unable to submit comments online, please mail written comments to:

Division of Dockets Management (HFA- 305)
Food and Drug Administration
5630 Fishers Lane, Rm. 1061
Rockville, MD 20852

All written comments should be identified with this document's docket number:


Issued by:
Guidance Issuing Office
Office of the Associate Commissioner for Regulatory Affairs

IOM Index 2019