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.). (2007). Guidance for industry: Pharmacogenomic data submissions, companion evidence. 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.
Chicago Style (17th ed.) CitationCenter for Drug Evaluation and Research (U.S.), National Center for Toxicological Research, Center for Biologics Evaluation and Research (U.S.), and Center for Devices and Radiological Health (U.S.). Guidance for Industry: Pharmacogenomic Data Submissions, Companion Evidence. 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.
MLA (9th ed.) CitationCenter for Drug Evaluation and Research (U.S.), et al. Guidance for Industry: Pharmacogenomic Data Submissions, Companion Evidence. 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.