- Additional Authors
- Description
- 25 p. : digital, PDF file.
- Alternative Title
- Pharmacogenomic data submissions, companion evidence
- Subject
- Pharmacogenomics > Government policy > United States
- Note
- Title from PDF title page (viewed on June 2, 2009).
- "Draft guidance".
- "Procedural".
- "August 2007".
- System Details (note)
- 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.
- Call Number
- GPO Internet HE 20.4702:P 49/10
- OCLC
- 368320454
- Title
Guidance for industry [electronic resource] : pharmacogenomic data submissions, companion evidence.
- Imprint
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]
- System Details
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.
- Connect to:
- Added Author
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.)
- Gpo Item No.
0499-T (online)
- Sudoc No.
HE 20.4702:P 49/10
- Research Call Number
GPO Internet HE 20.4702:P 49/10