Guidance for industry : providing regulatory submissions in electronic format, receipt date.

Format:

Book

Government document

Contributor:

Center for Drug Evaluation and Research (U.S.)

Center for Biologics Evaluation and Research (U.S.)

Language:

English

Subjects (All):

Electronic filing systems--Government policy--United States.

Electronic filing systems.

Drugs--Testing--Government policy--United States.

Drugs.

Biologicals--Evaluation--Government policy--United States.

Biologicals.

Drugs--Testing--Government policy.

United States.

Physical Description:

1 online resource (6 pages)

Other Title:

Providing regulatory submissions in electronic format, receipt date

Place of Publication:

Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [2007]

Notes:

Title from PDF title page (viewed on June 3, 2009).

"Draft guidance."

"June 2007."

OCLC:

369245702