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GUIDANCE DOCUMENT

Guideline for the Uniform Labeling of Blood and Blood Components August 1985

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

The information in this guideline is intended for any persons with responsibility for blood component labeling. The technical information contained in Section V should be of particular interest to label producers and designers of electronic data processing <EDP> systems used in a blood banking environment.


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.

Questions?

Contact Point
Office of Communication, Outreach and Development (OCOD)
Center for Biologics Evaluation and Research
Food and Drug Administration
10903 New Hampshire Ave WO71-3128
Silver Spring, MD 20993-0002
ocod@fda.hhs.gov
(800) 835-4709
(240) 402-8010