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Guidance for industry : compliance with 21 CFR part 1271.150(c)(1), manufacturing arrangements.

Bibliographic Details
Corporate Author: Center for Biologics Evaluation and Research (U.S.)
Format: Government Document eBook
Language:English
Published: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2006]
Subjects:
Human cell culture > Government policy > United States.
Tissue engineering > Government policy > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS112732
Description
Item Description:Title from PDF title page (viewed on May 18, 2009).
"September 2006".
Electronic resource.
Physical Description:i, 3 pages : digital, PDF file.
Format:Mode of access: Internet at the FDA CBER web site. Address as of 5/18/09: http://www.fda.gov/cber/gdlns/cgtpmanuf.pdf ; current access is available via PURL.
Bibliography:Includes bibliographical references (page 3).