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Information sheet guidance for sponsors, clinical investigators, and IRBs : frequently asked questions, statement of investigator (form FDA 1572).

Bibliographic Details
Corporate Author: United States. Food and Drug Administration
Format: Government Document eBook
Language:English
Published: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, [2008]
Subjects:
Medical research personnel.
Institutional review boards (Medicine)
Drug development.
Online Access:https://purl.fdlp.gov/GPO/LPS111644
Description
Item Description:Title from PDF title page (viewed on Apr. 21, 2009).
"Draft guidance."
"July 2008."
Electronic resource.
Physical Description:11 pages : digital, PDF file.
Format:Mode of access: Internet at the FDA Web site. Address as of 4/21/09: http://www.fda.gov/OHRMS/DOCKETS/98fr/FDA-2008-D-0406-gdl.pdf ; current access is available via PURL.