Guidance for industry : pharmacogenomic data submissions, companion evidence.

Bibliographic Details
Corporate Authors:	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.)
Format:	Government Document eBook
Language:	English
Published:	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]
Subjects:	Pharmacogenomics > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS113323

Description
Item Description:	"Draft guidance". "Procedural". "August 2007". Title from PDF title page (viewed on June 2, 2009). "Draft guidance." "Procedural." "August 2007." Electronic resource.
Physical Description:	25 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA web site. Address as of 6/2/09: http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM079855.pdf ; current access is available via PURL.