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Bioequivalence
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611	Title: E-BABE-Encyclopedia of Bioanalytical Methods for Bioavailability and Bioequivalence Studies of Pharmaceuticals Name: xxxxxxxx Stanford University School of Medicine, CA Add to Reading List Source URL: cancerscience2014.conferenceseries.net Language: English - Date: 2014-02-07 07:13:14 Pharmacokinetics Bioequivalence Bioavailability
612	Bioequivalence Studies Figure 1a Add to Reading List Source URL: www.fda.gov
613	Bioequivalence Studies Figure 2B Add to Reading List Source URL: www.fda.gov
614	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. This content has not been altered or updated since it was archived Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Bioequivalence Pharmacokinetics Center for Drug Evaluation and Research Abbreviated New Drug Application Pharmaceutical sciences Pharmacology Food and Drug Administration
615	______________________________________________________________________________ MEETING MINUTES ______________________________________________________________________________ SUBJECT: FDA-GPhA Board of Directors Quarterly Add to Reading List Source URL: www.fda.gov Language: English Pharmaceuticals policy Clinical research Pharmaceutical industry Generic drug Public domain Abbreviated New Drug Application Center for Drug Evaluation and Research Office of Regulatory Affairs Bioequivalence Pharmaceutical sciences Food and Drug Administration Pharmacology
616	FOOD AND DRUG ADMINISTRATION Center for Drug Evaluation and Research Advisory Committee for Pharmaceutical Science and Clinical Pharmacology (ACPS-CP) FDA White Oak Campus, Building 31, The Great Room (Rm[removed]White Oa Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Food and Drug Administration Clinical pharmacology Generic drug Bioequivalence Abbreviated New Drug Application Center for Drug Evaluation and Research Drug discovery Pharmaceutical sciences Pharmacology Pharmaceutical industry
617	Summary Minutes of the Advisory Committee for Pharmaceutical Science and Clinical Pharmacology April 14, 2010 Location: Hilton Silver Spring/Washington D.C., The Ballrooms, 8727 Colesville Road, Silver Spring, Maryland. Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceuticals policy Pharmaceutical industry Bioequivalence Generic drug Center for Drug Evaluation and Research Pharmaceutical sciences Pharmacology Food and Drug Administration
618	HEALTH CANADA USE ONLY Sponsors should address the points outlined below by answering “Yes”, “No”, or “Not Applicable”, providing a justification where required, and completing the requested information. This Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2014-01-13 12:58:35 Pharmaceutics Pharmacokinetics Clinical research Validity Abbreviated New Drug Application Bioequivalence Validation Bioavailability Verification and validation Pharmaceutical sciences Pharmaceutical industry Pharmacology
619	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. This content has not been altered or updated since it was archived Add to Reading List Source URL: www.fda.gov Language: English Clinical research Food and Drug Administration Bioequivalence Abbreviated New Drug Application Center for Drug Evaluation and Research Pharmaceutical sciences Pharmacology Pharmacokinetics
620	GDUF Negotiations Meeting[removed]PUBLIC Minutes Add to Reading List Source URL: www.fda.gov Language: English Clinical research Food and Drug Administration Pharmaceutical industry Center for Drug Evaluation and Research Generic drug Bioequivalence Mylan Prescription Drug User Fee Act Authorized generics Pharmaceutical sciences Pharmacology Pharmaceuticals policy

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