Guidance for sponsors, industry, researchers, investigators, and Food and Drug Administration staff : certifications to accompany drug, biological product and device applications/submissions : compliance with Section 402(j) of the Public Health Service Act, added by Title VIII of the Food and Drug Administration Amendments Act of 2007

Guidance for sponsors, industry, researchers, investigators, and Food and Drug Administration staff : certifications to accompany drug, biological product and device applications/submissions : compliance with Section 402(j) of the Public Health Service Act, added by Title VIII of the Food and Drug Administration Amendments Act of 2007.

Other author/creator	United States. Food and Drug Administration. Office of Policy.
Other author/creator	United States. Food and Drug Administration. Office of the Commissioner.
Format	Electronic and Book
Publication Info	Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of Policy : Office of the Commissioner, [2009]
Description	1 online resource (10 p.)
Supplemental Content	https://purl.fdlp.gov/GPO/LPS116943
Subject(s)	Drugs--Certification --Government policy --United States. Biological products--Certification --Government policy --United States. Medical instruments and apparatus--Certification --Government policy --United States.

Portion of title	Certifications to accompany drug, biological product and device applications/submissions
Portion of title	Compliance with Section 402(j) of the Public Health Service Act, added by Title VIII of the Food and Drug Administration Amendments Act of 2007
General note	"January 2009."
General note	GPO Cataloging Record Distribution Program (CRDP).
GPO item number	0475 (online)
Govt. docs number	HE 20.4702:C 33/2

Library	Location	Call Number	Status	Item Actions
Joyner	Electronic Resources	Access Content Online	✔ Available