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Bioequivalence
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171	SUBMISSION REQUIREMENTS CHECKLIST Add to Reading List Source URL: adstandards.com Language: English - Date: 2008-12-31 11:03:06 Pharmaceutical sciences Pharmaceutical industry Food and Drug Administration Design of experiments Clinical trial Drug Identification Number Bioequivalence Comparative advertising Clinical research Pharmacology Research
172	Request for RMS in a decentralised procedure, Add to Reading List Source URL: www.cbg-meb.nl Language: English - Date: 2015-04-17 16:22:23 Pharmaceutical industry Research Pharmaceuticals policy Bioequivalence Pharmacokinetics Active ingredient Supplementary protection certificate Clinical research Pharmaceutical sciences Pharmacology
173	Federal Register / Vol. 80, NoWednesday, April 15, Notices In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-04-15 10:56:33 Food and Drug Administration Pharmaceuticals policy Pharmaceutical industry Clinical research Center for Food Safety and Applied Nutrition Generic drug Bioequivalence Paperwork Reduction Act Dietary supplement Pharmaceutical sciences Pharmacology Health
174	Federal Register / Vol. 80, NoWednesday, March 18, Notices calculation of AAC adjusted by a multiplier of 1.1 for multiple source drugs and 1.01 for Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-03-18 02:25:06 Food and Drug Administration Clinical pharmacology Bioequivalence Pharmacokinetics Abbreviated New Drug Application Center for Veterinary Medicine Rulemaking In vitro Pharmaceutical industry Pharmaceutical sciences Pharmacology Clinical research
175	The Clinical Research Source Vol. 3, Issue 1 v Add to Reading List Source URL: www.aihealthsolutions.ca Language: English - Date: 2015-03-16 18:51:35 Health Pharmacology Pharmaceutical industry Medical statistics Food and Drug Administration Clinical trial Clinical investigator New Drug Application Bioequivalence Clinical research Research Pharmaceutical sciences
176	European Medicines Agency (EMA)/ European Generic medicines Association (EGA) Joint workshop on the impact of the revised EMA Guideline on the Pharmacokinetic and Clinical Evaluation of Modified Release Dosage Forms Add to Reading List Source URL: www.egaevents.org Language: English - Date: 2015-04-30 05:56:42 Pharmaceutical sciences Pharmaceutical industry Pharmacokinetics EMA European Medicines Agency Regulatory requirement Bioequivalence Clinical research Pharmacology Research
177	Paste your Logo here Paste your Photograph Here Add to Reading List Source URL: food.indoglobalsummit.com Language: English - Date: 2015-02-27 04:48:55 Scientific method Bioequivalence Bioavailability Pharmacopoeia High-performance liquid chromatography United States Pharmacopeia Bioanalysis Pharmacokinetics Chemistry Science
178	Public Assessment Report Scientific discussion Fluvastatin “Actavis” 20 mg and 40 mg hard capsules Add to Reading List Source URL: mri.medagencies.org Language: English - Date: 2015-05-08 19:04:25 Pharmaceutical sciences Chemistry Statin Fluvastatin Bioequivalence HMG-CoA reductase Capsule Excipient Clinical research Pharmaceutical industry Pharmacology
179	Missing Data Issues in Regulatory Clinical Trials Lisa M. LaVange, PhD Office of Biostatistics OTS/CDER/US FDA Add to Reading List Source URL: www.jpma.or.jp Language: English - Date: 2015-02-24 20:15:37 Clinical research Center for Drug Evaluation and Research Bioequivalence Center for Biologics Evaluation and Research Abbreviated New Drug Application Drug development Biologic Biostatistics Dermatologic and Ophthalmic Drugs Advisory Committee Food and Drug Administration Pharmaceutical sciences Pharmacology
180	Microsoft Word - PAR_1242_DC_22 mar 2010.doc Add to Reading List Source URL: db.cbg-meb.nl Language: English - Date: 2012-10-07 10:18:08 Pharmaceutical industry Lactams Bristol-Myers Squibb Irbesartan Angiotensin II receptor antagonist Bioequivalence Generic drug Drug Master File Aspirin Chemistry Organic chemistry Pharmacology

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