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Harmonisation
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#	Item
831	Microsoft PowerPoint - harmonisation_INS_BCEAO.ppt [Mode de compati Add to Reading List Source URL: www.afristat.org Language: French - Date: 2010-03-22 13:16:33
832	The ICH Global Cooperation Group (GCG) was formed on March 11, 1999, as a subcommittee of the ICH Steering Committee. Its purpose is to make information available on ICH, ICH activities, and ICH guidelines to any country Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:41:02 EMBnet Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry Clinical research IFPMA
833	The committee will discuss saxagliptin tablets, by Bristol-Myers Squibb, for the treatment of hyperglycemia in adults with type 2 diabetes mellitus Add to Reading List Source URL: www.fda.gov Language: English Drug safety Medicine Quality Quality by Design Food and Drug Administration United States Pharmacopeia Over-the-counter drug International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Monograph Pharmaceuticals policy Pharmacology Pharmaceutical sciences
834	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE November 2004 Revised June 2009 SEX-RELATED CONSIDERATIONS IN THE CONDUCT OF CLINICAL TRIALS 1 Preambl Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:41:38 Research Clinical research Drug safety Drug discovery Clinical trial Pharmacovigilance Food and Drug Administration Drug development New Drug Application Pharmaceutical sciences Pharmacology Pharmaceutical industry
835	Microsoft Word - ICH SC Meeting Chicago Summary Final, August 16, 2006.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:45:56 Science Pharmaceutical sciences Clinical Data Management Pharmaceuticals policy Pharmaceutical industry MedDRA Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Common Technical Document Clinical research Research Pharmacology
836	ICH STEERING COMMITTEE[removed]June 2011 Cincinnati, OH, USA SUMMARY 1. Opening Discussions The ICH Steering Committee (SC) meeting in Cincinnati was chaired by FDA. The Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:15 Electronic Common Technical Document Pharmaceutical industry MedDRA Environmental Working Group Quality by Design Common Technical Document International Organization for Standardization International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical Data Management Clinical research Research
837	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE 25 October 2006 ICH Considerations General Principles to Address the Risk of Inadvertent Germline Inte Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:33 Applied genetics Medical genetics Medical research Viral vector Gene therapy Vector Retrovirus Lentivirus Oncolytic virus Biology Molecular biology Gene delivery
838	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE GLOBAL COOPERATION GROUP MEETING REPORT TUESDAY OCTOBER 27, 2009 St. Louis, MO, USA Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:44:20 Pharmaceutical industry Health Pharmaceuticals policy Pharmacology Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA IFPMA Electronic Common Technical Document Clinical research Research Pharmaceutical sciences
839	Microsoft Word - ICH SC Meeting Brussels 2008-summary.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:45:56 Science Health Pharmaceuticals policy Drug safety Clinical Data Management International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA Electronic Common Technical Document Environmental Working Group Clinical research Research Pharmacology
840	Microsoft Word - ICH SC Meeting St. Louis 2009.doc Add to Reading List Source URL: www.ich.org Language: English Medicine Pharmacology Medical informatics Drug safety Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document MedDRA Environmental Working Group Clinical research Health Research