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Bioequivalence
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871	We Take Intensive Care Of Your Biosimilar Investigational Product Combining Safety And Capacity With High Standards Expertise In GxP GCP is the basis for all clinical activities and was successfully confirmed during insp Add to Reading List Source URL: www.crs-group.de Language: English - Date: 2014-04-04 07:50:35 Pharmaceutical industry Science Design of experiments Pharmacology Clinical trial Bioequivalence Clinical research Research Pharmaceutical sciences
872	A novel approach to testing for bioequivalence based on modeling the within-period dependence structure Rameela Chandrasekhar1 , Alan D. Hutson1 and Gregory E. Wilding1∗ 1 Add to Reading List Source URL: sphhp.buffalo.edu Language: English - Date: 2014-07-04 07:13:17 Pharmacokinetics Regression analysis Bioequivalence Clinical research Parametric statistics Abbreviated New Drug Application Generic drug Sample size determination Statistical power Statistics Pharmaceutical sciences Pharmacology
873	Female Scientific Research Team With Clear Solution In Laboratory Add to Reading List Source URL: www.egagenerics.com Language: English Pharmaceutics Pharmaceutical industry Clinical research Pharmaceuticals policy Bioequivalence Abbreviated New Drug Application Generic drug Dissolution testing Regulatory requirement Pharmaceutical sciences Pharmacology Pharmacokinetics
874	Microsoft Word - Guidance Agenda 2012_080712.doc Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Drug safety Clinical research Pharmaceutical industry Abbreviated New Drug Application Bioequivalence Investigational New Drug Center for Drug Evaluation and Research New Drug Application Pharmaceutical sciences Pharmacology Medicine
875	Guidance for Industry Submission of Summary Bioequivalence Data for ANDAs U.S. Department of Health and Human Services Food and Drug Administration Add to Reading List Source URL: www.fda.gov Language: English Clinical research Research Bioequivalence Excipient Abbreviated New Drug Application Generic drug Food and Drug Administration New Drug Application Time release technology Pharmaceutical sciences Pharmaceutical industry Pharmacology
876	Microsoft Word - Pathway_Regulatory_Oct09.doc Add to Reading List Source URL: www.arcs.com.au Language: English - Date: 2012-06-07 03:19:54 Pharmacology Clinical Data Management Pharmacokinetics Electronic Common Technical Document Common Technical Document Bioequivalence Regulatory affairs Bioavailability Pharmaceutical industry Pharmaceutical sciences Clinical research Research
877	WORLD COURIER BIO SEMINAR SERIES CLINICAL TRIALS FROM DIFFERENT PERSPECTIVES Dear Partners, Add to Reading List Source URL: www.worldcourier.com Language: English - Date: 2014-05-20 05:40:26 Pharmacology Snagov Clinical trial Bioequivalence Fulga Clinical research Research Pharmaceutical sciences
878	Microsoft Word - Comprehensive List Of Guidances_3[removed]doc Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmacokinetics Pharmaceuticals policy Bioequivalence Food and Drug Administration Generic drug Dissolution testing Abbreviated New Drug Application Biopharmaceutics Classification System Pharmaceutical sciences Pharmacology Pharmaceutical industry
879	Pharmacokinetic Assessment of Two Extended Release Prescription Products Add to Reading List Source URL: www.fda.gov Language: English Organochlorides Stimulants Bupropion Cathinones GlaxoSmithKline Texas Tech University Health Sciences Center Methadone Antidepressant Bioequivalence Chemistry Pharmacology Pharmaceutical sciences
880	Division of Bioequivalence Review of Pharmacokinetic and Dissolution Data Add to Reading List Source URL: www.fda.gov

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