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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
Results: 311

#	Item
31	Electronic Transmission of Individual Case Safety Reports Message Specification Document Version 2.3 November 9, 2000 INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICAL Add to Reading List Source URL: estri.org Language: English - Date: 2012-06-05 01:13:02 Technology Information Standard Generalized Markup Language International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use HTML Document Type Definition Health Level 7 Electronic data interchange Uniform resource identifier Computing Markup languages Technical communication
32	Recommendation Notebook Version 3.0 ICH M2 Electronic Standards for the Transfer of Regulatory Information Add to Reading List Source URL: estri.org Language: English - Date: 2012-06-05 01:13:02 Environmental Working Group Food and Drug Administration International standard Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical research Research Pharmaceutical sciences
33	Electronic Transmission of Individual Case Safety Reports Message Specification Document Version 2.3 November 9, 2000 Electronic Transmission of Individual Case Safety Reports Message Specification Document Version 2.3 Add to Reading List Source URL: estri.org Language: English - Date: 2012-06-05 01:13:02 Standard Generalized Markup Language Document Type Definition XML HTML International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic data interchange Computing Markup languages Technical communication
34	LOGO CE_horizontal_EN_quadri Add to Reading List Source URL: www.ich.org Language: English - Date: 2015-02-20 08:31:27 Pharmaceutical sciences Pharmacology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use European Medicines Agency Good Clinical Practice European Federation of Pharmaceutical Industries and Associations Clinical trial Dia Clinical research Pharmaceutical industry Research
35	29 January[removed]MEETING REPORT ICH Steering Committee 12 – 13 November 2014, Lisbon, Portugal Add to Reading List Source URL: www.ich.org Language: English - Date: 2015-01-29 03:32:29 Pharmaceutical sciences Pharmaceuticals policy Pharmaceutics Clinical Data Management Pharmacology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document MedDRA Common Technical Document Clinical research Research Pharmaceutical industry
36	[removed]Federal Register / Vol. 80, No[removed]Monday, March 9, [removed]Notices shall provide such person a written statement of the classification (if any) of such device and the requirements of the Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-03-09 13:45:45 Health Food and Drug Administration Pharmaceuticals policy Pharmaceutical industry Drug safety New Drug Application Bioequivalence International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Medical device Medicine Clinical research Pharmaceutical sciences
37	mstockstill on DSK4VPTVN1PROD with NOTICES[removed]Federal Register / Vol. 80, No[removed]Monday, March 9, [removed]Notices Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2015-03-09 13:45:45 Pharmaceutical sciences Pharmaceutical industry Clinical research National Institutes of Health Pharmacology National Institute of Diabetes and Digestive and Kidney Diseases Validation Food and Drug Administration International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceuticals policy Medicine Health
38	Microsoft Word - A_SSFFC_WG2-en.doc Add to Reading List Source URL: apps.who.int Language: English - Date: 2012-10-11 04:02:06 Pharmaceuticals policy Health Drug safety Clinical research International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacovigilance Essential medicines Pharmaceutical industry Good manufacturing practice Pharmaceutical sciences Pharmacology Pharmacy
39	WORLD HEALTH ORGANIZATION FIFTY-SEVENTH WORLD HEALTH ASSEMBLY Provisional agenda item[removed]A57[removed]April 2004 Add to Reading List Source URL: apps.who.int Language: English - Date: 2012-02-13 07:30:18 Pharmaceutical industry Pharmacy Clinical research Pharmaceuticals policy Good manufacturing practice Clinical trial Phytotherapy European Medicines Agency International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmacology Health
40	PHARMACEUTICAL INSPECTION CONVENTION PHARMACEUTICAL INSPECTION CO- OPERATION SCHEME 2 February 2015 EMA/INS/GMP[removed] Add to Reading List Source URL: www.picscheme.org Language: English - Date: 2015-02-10 05:55:58 Good manufacturing practice Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme Business EudraLex Quality management system Technology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry Pharmaceuticals policy Health