Research Catalog

Title

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

Publication

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, [2008]

Details

Additional Authors

United States. Food and Drug Administration.

Description

11 pages : digital, PDF file

Subject

• Medical research personnel
• Institutional review boards (Medicine)
• Drug development

Note

• Title from PDF title page (viewed on Apr. 21, 2009).
• "Draft guidance."
• "July 2008."

System Details (note)

• 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.

Call Number

GPO Internet HE 20.4802:IN 4

OCLC

marcive318920509

Title

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

Publisher

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, [2008]

Type of Content

text

Type of Medium

computer

Type of Carrier

online resource

System Details

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.

Connect to:

https://purl.fdlp.gov/GPO/LPS111644

Added Author

United States. Food and Drug Administration.

Gpo Item No.

0499-T-02 (online)

Sudoc No.

HE 20.4802:IN 4