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GUIDANCE DOCUMENT

Providing Regulatory Submissions in Electronic Format--Receipt Date Guidance for Industry February 2014

Download the Final Guidance Document
Final
Docket Number:
FDA-2007-D-0077
Issued by:
Guidance Issuing Office
Center for Drug Evaluation and Research
Center for Biologics Evaluation and Research

This is one in a series of guidance documents intended to assist sponsors, applicants, and others making regulatory submissions to the Food and Drug Administration (FDA) in electronic format.

Submit Comments

Submit Comments Online

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-2007-D-0077.

 
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