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E-REPORT
Title Guidance for industry [electronic resource] : gene therapy clinical trials, observing subjects for delayed adverse events.
Imprint Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, [2006]

Copies/Volumes

LOCATION CALL # STATUS
 Internet  Electronic Report    AVAILABLE
Description i, 23 p. : digital, PDF file.
Note Title from PDF title page (viewed on May 12, 2009).
"November 2006".
Bibliog. Includes bibliographical references (p. 23).
Note 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.
Subject Gene therapy -- United States.
Clinical trials -- Government policy -- United States.
Other Author Center for Biologics Evaluation and Research (U.S.)
Other Title Gene therapy clinical trials, observing subjects for delayed adverse events.