Impurity - PDFSEARCH.IO - Document Search Engine

Impurity
Results: 201

#	Item
151	Compendial Deferrals for USP37-NF32 1S Category Monograph Title Monograph Section Add to Reading List Source URL: www.usp.org Language: English - Date: 2013-11-18 13:18:16 Standards Verification and validation Chemical substance Impurity Ethanol USP Water Reagent Assay Chemistry Drugs Drug reference standard
152	Compendial Cancellations for USP37-NF32 1S Category Monograph Title Monograph Section Add to Reading List Source URL: www.usp.org Language: English - Date: 2013-11-18 13:18:16 Product certification Drug reference standard Standards Impurity Chemical substance USP Organic food Ethanol Chemistry Drugs Pharmacology
153	Q3A(R): Impurities in New Drug Substances Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-12 14:26:04 Pharmaceutical sciences Clinical research Pharmaceuticals policy Validity Validation Impurity Good manufacturing practice Health Canada Methamphetamine Pharmaceutical industry Medicine Pharmacology
154	Compendial Approvals to USP37-NF32 Category Monograph Title Section Head Add to Reading List Source URL: www.usp.org Language: English - Date: 2013-07-19 15:52:49 Pharmaceutical industry Quality management Systems engineering Validity Verification and validation Drug reference standard USP Glycine Impurity Chemistry Science Food safety
155	Observations of an Impurity-driven Hysteresis Behavior in Ice Crystal Growth at Low Pressure Kenneth G. Libbrecht1 Department of Physics, California Institute of Technology Pasadena, California 91125 Add to Reading List Source URL: www.its.caltech.edu Language: English - Date: 2008-09-28 14:42:08 Mineralogy Laboratory techniques Separation processes Crystallization Crystal growth Crystal Ice Nucleation Freezing Chemistry Phase transitions Crystallography
156	ORIGINAL 001E8 NOT CONTAIN CBI Syngenta Crop Protection, LLC P.O. Box 18300 Add to Reading List Source URL: www.epa.gov Language: English - Date: 2013-01-10 16:53:20 Impurity Business 94th United States Congress Toxic Substances Control Act Syngenta
157	ORIGINAL 001E8 NOT CONTAIN CBI Syngenta Crop Protection, LLC P.O. Box 18300 Add to Reading List Source URL: www.epa.gov Language: English - Date: 2013-01-14 12:19:52 Impurity Business 94th United States Congress Toxic Substances Control Act Syngenta
158	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED T RIPARTITE GUIDELINE ASSESSMENT AND CONTROL OF DNA REACTIVE (MUTAGENIC) Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-07-15 04:10:52 Euphoriants Pharmacology Pharmaceuticals policy Carcinogenesis Mutagen Mutation Monoclonal antibodies Methamphetamine Impurity Medicine Biology Health
159	Cadmium imported as a component of lead and zinc concentrates, in cadmium commodities of unknown metal content, and as an impurity in other imported metals or alloys.(3) Cadmium is used primarily for electroplating othe Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-07-09 12:16:54 Toxicology Chemical elements Transition metals Cadmium poisoning Heavy metal Itai-itai disease Zinc Median lethal dose Mercury Chemistry Matter Cadmium
160	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE Final Concept Paper M7: Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceutica Add to Reading List Source URL: www.ich.org Language: English - Date: 2013-09-16 08:48:10 Clinical research Pharmaceuticals policy Environmental chemistry Impurity Materials Food and Drug Administration International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Genotoxicity Carcinogen Medicine Health Carcinogenesis

UPDATE