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Trial master file
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11	DRS eTMF News Release_022513 Add to Reading List Source URL: www.drscorp.com Language: English - Date: 2013-10-10 11:13:30 DRS Electronic trial master file
12	CASE STUDY DRS Professional Services: Trial Master File (TMF) Management DRS streamlines TMF management for Fortune 250 company; speeds turnaround time; lowers costs; and helps develop better workflow with CRO vendors Add to Reading List Source URL: www.drscorp.com Language: English - Date: 2013-10-10 11:13:30 Electronic trial master file Document management system Clinical trial Research Clinical research Science
13	The Study Site Master File and Essential Documents Standard Operating Procedure Office of Health and Medical Research Queensland Health Add to Reading List Source URL: www.health.qld.gov.au Language: English - Date: 2013-10-01 01:47:32 Science Pharmaceutical sciences Design of experiments Pharmacology Clinical research coordinator Clinical trial Institutional review board Good Clinical Practice Case report form Clinical research Research Pharmaceutical industry
14	Version July[removed]PROTECTED ` Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-06-24 11:49:04 Pharmaceutical sciences Pharmacology Validity Food and Drug Administration Validation Abbreviated New Drug Application Clinical trial Drug Master File Methamphetamine Pharmaceutical industry Clinical research Pharmaceutics
15	Microsoft Word - ctd_prep_rev_nds-eng.doc Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2014-06-17 11:30:03 Research Technology Pharmaceutical industry Medical informatics Electronic Common Technical Document Common Technical Document Global Harmonization Task Force Drug Master File Clinical trial Medicine Clinical research Clinical Data Management
16	Master File System for Drug Substances, etc. 1. Master File (MF) System Master file (hereinafter referred to as “MF”) system for drug substances, etc. allows Japanese or foreign manufacturers of drug substances etc. Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2013-06-09 22:47:17 Health Pharmaceutical industry Marketing authorization Generic drug Over-the-counter drug Clinical trial Medical prescription Pharmaceutical sciences Pharmaceuticals policy Pharmacology
17	GUIDANCE FOR INDUSTRY PREPARATION OF VETERINARY NEW DRUG SUBMISSIONS VETERINARY DRUGS DIRECTORATE HEALTH CANADA Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-07-26 15:35:35 Pharmacology Research Pharmaceutics Food and Drug Administration Pharmaceuticals policy Regulatory requirement Drug Master File Validation Clinical trial Pharmaceutical industry Pharmaceutical sciences Clinical research
18	Version July[removed]PROTECTED ` Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:49:04 Pharmaceutical sciences Pharmacology Validity Food and Drug Administration Validation Abbreviated New Drug Application Clinical trial Drug Master File Methamphetamine Pharmaceutical industry Clinical research Pharmaceutics
19	DOC Document Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-06-24 11:39:21 Clinical research Research Science Food and Drug Administration Drug Master File Pharmaceutical formulation Clinical trial Abbreviated New Drug Application Excipient Pharmacology Pharmaceutical industry Pharmaceutical sciences
20	Microsoft Word - draft_ebauche_dmf_fmm_guide_ld-eng.doc Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-07-12 14:25:40 Medicine Pharmaceutics Clinical research Drug Master File Pharmacology Natural Health Products Clinical trial Health Products and Food Branch Guidance document Pharmaceutical industry Health Canada Health

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