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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
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101	[removed]Federal Register / Vol. 65, No[removed]Thursday, May 4, [removed]Notices Management Branch, Procurement and Grants Office, Centers for Disease Add to Reading List Source URL: www.fda.gov Language: English - Date: 2000-05-04 05:29:31 Pharmaceuticals policy Pharmaceutical industry Common Technical Document Regulatory requirement Food and Drug Administration IFPMA Nuisance Pharmaceutical Research and Manufacturers of America International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences clinical research Pharmacology
102	PRESS RELEASE Invitation to Submit an Expression of Interest for the MSSO Tender Geneva, February 10, 2014 – The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals f Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-02-10 03:59:08 MedDRA Drug safety Research Pharmaceutical sciences International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry Science Clinical research Pharmacology Pharmaceuticals policy
103	The Evolution of ICH Shift From Input to Output-The Influence of the CTD Justina A. Molzon, MS Pharm, JD Associate Director for International Programs Center for Drug Evaluation and Research US Food and Drug Administrati Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:30 Clinical research Clinical Data Management Pharmaceutical industry Electronic Common Technical Document MedDRA IFPMA Food and Drug Administration International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Common Technical Document Pharmaceutical sciences Research Pharmacology
104	Microsoft PowerPoint - _Special - Morin - ICH [Compatibility Mode] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:08:38 Pharmaceutical industry Health Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacology Japan Pharmaceutical Manufacturers Association Clinical trial IFPMA Clinical research Research Pharmaceutical sciences
105	Microsoft PowerPoint - 5) Pharmacopeia_SK.ppt [Compatibility Mode] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:05:51 European Directorate for the Quality of Medicines Strasbourg European Pharmacopoeia Medicine Europe Pharmaceuticals policy Health International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use European Union Council of Europe Pharmacopoeias Homeopathy
106	Microsoft PowerPoint - Breakout B CS Summary.ppt [Compatibility Mode] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:05:50 Pharmaceuticals policy Association of Southeast Asian Nations Clinical research Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
107	ICH and EU regulatory framework and the role of the European Medicines Agency (EMA) ASEAN Training Workshop on ICH Q5C[removed]May 2011, Kuala Lumpur Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:42:25 Pharmaceutical sciences Pharmaceutics Clinical Data Management Pharmacology Common Technical Document IFPMA International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use European Medicines Agency Japan Pharmaceutical Manufacturers Association Clinical research Pharmaceutical industry Research
108	Draft Guidance Document - Preparatin of Drug Regulatory Activities in the Electronic Common Technical Document Format Add to Reading List Source URL: hc-sc.gc.ca Language: English - Date: 2013-07-09 17:16:48 Technology Clinical Data Management Pharmaceutical industry Pharmaceuticals policy Drug safety Electronic Common Technical Document Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Drug Master File Medicine Clinical research Research
109	ICH M4: Common Technical Document Modules IIA, IIB Nonclinical; Module III, Quality; Modules IV, Nonclinical; Module V, Efficacy Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Pharmacology Clinical Data Management Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Nonclinical studies Clinical trial Executive summary Electronic Common Technical Document Clinical research Research Drug discovery
110	Microsoft PowerPoint - Workshop D - Pharmacopoeial.ppt [Compatibility Mode] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:05:58 European Pharmacopoeia Homeopathy Kuala Lumpur International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Health Government Pharmacopoeias Medicine Council of Europe