Guidance for industry : pharmacogenomic data submissions, companion guidance.

Format:

Book

Government document

Contributor:

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

National Center for Toxicological Research

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

Center for Devices and Radiological Health (U.S.)

Language:

English

Subjects (All):

Pharmacogenomics--Government policy--United States.

Pharmacogenomics.

United States.

Physical Description:

1 online resource (25 pages)

Other Title:

Pharmacogenomic data submissions, companion evidence

Place of Publication:

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

Notes:

Title from PDF title page (viewed on June 2, 2009).

"Draft guidance."

"Procedural."

"August 2007."

OCLC:

368320454