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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
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91	-- Bert spiker, PhD, MD SENIOR VICE PRESIDENT SClENl.lflC AND REQUIATORY AFFAIRS .* Add to Reading List Source URL: www.fda.gov Language: English - Date: 2000-11-15 00:43:10 Science Common Technical Document Pharmaceutical industry Evaluation methods Clinical trial Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical research Research Clinical Data Management
92	Understanding MedDRA The Medical Dictionary for Regulatory Activities What is ICH? The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) (www.ich Add to Reading List Source URL: www.ich.org Language: English - Date: 2013-09-17 11:47:48 Research Clinical research Drug safety Pharmaceutical industry Pharmaceuticals policy MedDRA EudraVigilance IFPMA Pharmacovigilance Pharmacology Pharmaceutical sciences Health
93	Implementation of ICH Q8, Q9, Q10 Breakout D : Pharmacopoieal Requirements and the New ICH Quality Paradigm – Time for a Change? Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:05:51 International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacopoeia Kuala Lumpur Alternative medicine Software development process Process analytical technology Form Research Quality Quality by Design Science
94	Merck& Co..Inc. TwoBethesda MetroCenter MerckResearch laboratories Suite700 Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-11-10 09:50:33 Clinical research Pharmaceutical industry Food and Drug Administration United States Public Health Service Clinical trial Biologic Merck & Co. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences Pharmacology Research
95	MedDRA: an ICH Success Story ASEAN MedDRA Training Kuala Lumpur, March 17-19, 2010 Dr. Christina Winter, Medical Director Global Clinical Safety & Pharmacovigilance Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:09 Clinical research Health Drug safety Pharmaceutical industry Pharmacy MedDRA IFPMA International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Japan Pharmaceutical Manufacturers Association Pharmacology Pharmaceutical sciences Research
96	Progressive Licensing and the Modernization of the Canadian Regulatory Framework Workshop on Implementation of ICH Quality Guidelines Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:18 Clinical research Public administration Law Pharmaceuticals policy United States administrative law Technology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Economics of regulation Administrative law Regulation
97	PRESS RELEASE Minneapolis, MN, USA, ICH MedDRA® Management Board Meeting ICH MedDRA Management Board Supports MedDRA’s Continuing Evolution Minneapolis, 1 June 2014 – The MedDRA Management Board met in Minneapolis, Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-06-24 10:22:26 Drug safety Clinical research International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Research Science Health Pharmacology MedDRA Pharmaceuticals policy
98	PRESS RELEASE Osaka, Japan, November 2013 “ICH Reviews Future ICH Topics and Its Organisation Towards Increased Engagement Globally” The International Conference on Harmonisation (ICH) Steering Committee (SC) and its Add to Reading List Source URL: www.ich.org Language: English - Date: 2013-12-02 10:38:34 Pharmaceutical sciences Health Pharmaceutical industry Pharmacology Clinical Data Management International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA Common Technical Document Ich will Clinical research Research Pharmaceuticals policy
99	Animal Use for Testing Purposes Drug Development Process PHARMACOLOGY Complete Drug Efficacy / Add to Reading List Source URL: www.ccac.ca Language: English - Date: 2013-01-31 13:22:23 Pharmaceutical industry Clinical research Drug discovery Pharmacology Pharmaceuticals policy Pre-clinical development Drug development Clinical trial International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Research Pharmaceutical sciences Science
100	Criteria / Considerations to Participate in the ICH Global Cooperation Session of the Steering Committee The ICH Steering Committee (SC) has invited Regional Harmonisation Initiatives (RHIs) and Drug Regulatory Authoriti Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-03-17 09:20:58 Clinical research Research International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use