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GUIDANCE DOCUMENT

Real World Data / Real World Evidence RWD/RWE July 2018

Final
Issued by:
Guidance Issuing Office
Center for Drug Evaluation and Research

Use of Electronic Health Record Data in Clinical Investigations Guidance for Industry


Submit Comments

Submit comments on this guidance document electronically via docket ID: FDA-2013-S-0610 - Specific Electronic Submissions Intended For FDA's Dockets Management Staff (i.e., Citizen Petitions, Draft Proposed Guidance Documents, Variances, and other administrative record submissions)

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 comments should be identified with the title of the guidance.

 
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