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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
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https://purl.fdlp.gov/GPO/LPS113323

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Call Number: HE 20.4702:P 49/10
 
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HE 20.4702:P 49/10 Available
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