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Bioequivalence
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321	Guidance note to Manufacturers on the compilation of the Add to Reading List Source URL: apps.who.int Language: English - Date: 2008-06-23 08:16:46 Abbreviated New Drug Application Bioequivalence
322	Clinical Pharmacology Program for Polypill Cardiovascular and Renal Drugs Advisory Committee Meeting September 10, 2014 Sudharshan Hariharan, Ph.D. Division of Clinical Pharmacology-I Add to Reading List Source URL: www.fda.gov Language: English Medicine Polypill Pharmacokinetics Pharmacy Medicinal chemistry Bioequivalence Aspirin Clinical pharmacology Pharmacodynamics Pharmacology Pharmaceutical sciences Drugs
323	Recommended list of comparator products for anti-tuberculosis medicines invited by the WHO Prequalification of Medicines programme Add to Reading List Source URL: apps.who.int Language: English - Date: 2008-04-25 02:50:18 Pharmacokinetics Sesquiterpenes Organochlorides Artemether Alcohols Artemisinin Dihydroartemisinin Bioequivalence Lumefantrine Chemistry Pharmacology Pharmaceutical sciences
324	Date of Approval: October 14, 2014 FREEDOM OF INFORMATION SUMMARY ORIGINAL ABBREVIATED NEW ANIMAL DRUG APPLICATION ANADA[removed] Add to Reading List Source URL: www.fda.gov Language: English Flunixin Norbrook Organofluorides Bioequivalence Non-steroidal anti-inflammatory drug Meglumine Schering-Plough Pharmacology Pharmacokinetics Pharmaceutical sciences
325	CDER Bioequivalence Recommendations Withdrawn Listing 2014 Title Type Add to Reading List Source URL: www.fda.gov
326	Note to applicants expressing interest for supplying artemisinin containing drug products: Add to Reading List Source URL: apps.who.int Language: English - Date: 2006-11-21 08:36:58 Health Pharmaceutical industry Design of experiments Clinical Data Management Common Technical Document Clinical trial Artemisinin Malaria Bioequivalence Clinical research Medicine Research
327	IPEC Americas –FDA-OGD Meeting, Inactive Ingredient Database (IID) Add to Reading List Source URL: www.fda.gov Language: English Clinical research Food and Drug Administration Therapeutics United States Public Health Service Bioequivalence Center for Drug Evaluation and Research Pharmaceutical sciences Pharmacology Research
328	Methylphenidate Hydrochloride Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Bioequivalence Bioavailability Methylphenidate Dissolution testing American University in Cairo Pharmacology Pharmacokinetics Pharmaceutical sciences
329	Microsoft Word[removed]Aug 19 - IPEC_GPhA_ FDA-OGD Conference call FINAL.docx Add to Reading List Source URL: www.fda.gov Language: English Clinical research Pharmaceutical industry Food and Drug Administration United States Public Health Service Generic drug Center for Drug Evaluation and Research Bioequivalence Environmental Working Group Pharmaceutical sciences Pharmacology Pharmaceuticals policy
330	Federal Register / Vol. 79, No[removed]Thursday, November 6, [removed]Notices SUPPLEMENTARY INFORMATION: I. Background In the Federal Register of June 11, [removed]FR 33311), FDA announced the Add to Reading List Source URL: osp.od.nih.gov Language: English - Date: 2014-11-07 15:34:36 Government Biosecurity Public comment Federal Register Methylphenidate Food and Drug Administration Bioequivalence Pharmacology United States administrative law Pharmaceutical sciences

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