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Dissolution testing
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31	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Bioequivalence Pharmacokinetics Dissolution testing Pyrimethamine Abbreviated New Drug Application Generic drug Chemistry Research Antimalarial medication Pharmaceutical industry Pharmacology Clinical research
32	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Quality control Topiramate Chemistry Bioequivalence Alcoholism Abbreviated New Drug Application Pharmaceutical sciences Pharmacology Dissolution testing Pharmaceutical industry
33	Contains Nonbinding Recommendations Draft Guidance on Loperamide Hydrochloride This draft guidance, once finalized, will represent the Food and Drug Administration’s (FDA’s) current thinking on this topic. It does n Add to Reading List Source URL: www.fda.gov Language: English Quality control Bioequivalence Pharmaceutical sciences Research Combination drugs Pharmacology Dissolution testing Pharmaceutical industry
34	DOCX Document Add to Reading List Source URL: mrh.eac.int Language: English - Date: 2014-01-25 14:41:08 Pharmaceutics Clinical research Pharmaceutical industry Bioequivalence Medicinal chemistry Abbreviated New Drug Application Bioavailability Biopharmaceutics Classification System Dissolution testing Pharmaceutical sciences Pharmacology Pharmacokinetics
35	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Pharmaceutical industry Anticonvulsants Mood stabilizers Dibenzazepines Bioequivalence Carbamazepine Dissolution testing Abbreviated New Drug Application Pharmacology Pharmaceutical sciences Pharmacokinetics
36	RTF Document Add to Reading List Source URL: mrh.eac.int Language: English - Date: 2014-01-25 14:40:18 Pharmacokinetics Analytical chemistry Bioequivalence Clinical research Equilibrium chemistry PH Dissolution testing Abbreviated New Drug Application Matrix Chemistry Pharmaceutical sciences Pharmacology
37	Guidance for Industry Bioavailability and Bioequivalence Studies for Orally Administered Drug Products - General Considerations Add to Reading List Source URL: www.fda.gov Language: English - Date: 2002-07-10 10:01:47 Pharmaceutics Pharmaceutical industry Clinical research Pharmaceuticals policy Bioequivalence Bioavailability Abbreviated New Drug Application Regulatory requirement Dissolution testing Pharmaceutical sciences Pharmacology Pharmacokinetics
38	An Assessment of Impediments to Competition in the Pharmaceutical Sector in Jamaica: Supplementary Volume: Comparative In Vitro Dissolution and Biopharmaceutical Properties of Some Multi-Source Antihypertensive Drug Prod Add to Reading List Source URL: idl-bnc.idrc.ca Language: English - Date: 2011-09-02 02:05:49 Pharmaceuticals policy Clinical research Pharmacokinetics Abbreviated New Drug Application Bioequivalence Generic drug Food and Drug Administration Dissolution testing Regulatory requirement Pharmaceutical sciences Pharmacology Pharmaceutical industry
39	DIVISION OF BIOEQUIVALENCE REVIEW Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutics Aripiprazole Bioequivalence Cmax Dissolution testing Antipsychotic Generic drug Bioavailability Abbreviated New Drug Application Pharmacokinetics Pharmacology Pharmaceutical sciences
40	Compendial Deferrals to USP37-NF32 Monograph Title Section Head <5> INHALATION AND NASAL DRUG PRODUCTS Add to Reading List Source URL: www.usp.org Language: English - Date: 2015-01-07 12:29:13 Drug reference standard Drugs Standards Verification and validation Chemical substance Dissolution testing USP Assay Impurity Chemistry Pharmaceutical industry Science