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Guidance for industry : gene therapy clinical trials, observing subjects for delayed adverse events.

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:
Gene therapy > United States.
Clinical trials > Government policy > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS112486
Description
Item Description:Title from PDF title page (viewed on May 12, 2009).
"November 2006".
Electronic resource.
Physical Description:i, 23 pages : digital, PDF file.
Format:Mode of access: Internet at the FDA CBER web site. Address as of 5/12/09: http://www.fda.gov/cber/gdlns/gtclin.pdf ; current access is available via PURL.
Bibliography:Includes bibliographical references (page 23).