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291	Microsoft Word - ICH SC Summary Chicago 2006 Draft 3 with links.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:44 Pharmacology Pharmaceutical sciences Science Pharmaceuticals policy Quality International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document MedDRA Quality by Design Clinical research Research Pharmaceutical industry
292	Microsoft Word - Final ICH SC Summary Brussels 2007_with links.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:45 Research Medicine Health MedDRA Electronic Common Technical Document Environmental Working Group Quality by Design International Organization for Standardization ISO 10303 Pharmacology Clinical research Pharmaceuticals policy
293	ICH STEERING COMMITTEE November 6-11, 2010 Fukuoka, Japan SUMMARY 1. Opening Discussions The ICH Steering Committee (SC) meeting in Fukuoka was chaired by MHLW. The Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:14 Medicine Research Drug safety Medical informatics Pharmaceuticals policy Electronic Common Technical Document MedDRA Environmental Working Group Fukuoka Health Clinical research Pharmacology
294	Microsoft Word - ICH SC Meeting Tallinn 2010.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:46 Pharmaceuticals policy MedDRA Medicine Drug safety Electronic Common Technical Document Environmental Working Group Health International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical research Research Pharmacology
295	Microsoft Word - ICH SC Statement 1990.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:41:18 Science International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical trial Harmonisation of law MedDRA Clinical research Research Health
296	Ref: GCG 167F GLOBAL COOPERATION GROUP MEETING FINAL REPORT TUESDAY NOVEMBER 13, 2012 San Diego, CA, USA (Hilton Bayfront Hotel) Add to Reading List Source URL: www.ich.org Language: English - Date: 2013-07-04 08:38:15 Science Clinical research Pharmacology Clinical Data Management Pharmaceuticals policy Good manufacturing practice Accelrys EMBnet MedDRA Pharmaceutical industry Pharmaceutical sciences Research
297	Microsoft Word - GCG132F_Final Report GCG_Meeting_Fukuoka_November 2010.docx Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:44:23 Research Pharmaceutics Pharmaceuticals policy Pharmacology Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA EMBnet IFPMA Pharmaceutical industry Clinical research Pharmaceutical sciences
298	Overview of ICH International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Overview of ICH Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-01-08 03:50:59 International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document Common Technical Document MedDRA Clinical trial Pharmacopoeia Clinical research Research Science
299	Microsoft Word - ICH SC Meeting Yokohama 2009_Without URL.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:45 Science Health Pharmaceuticals policy Drug safety Clinical Data Management Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA Environmental Working Group Clinical research Research Pharmacology
300	Microsoft Word - GCG140F Final Report GCG_Meeting_Cincinnati_June 2011.docx Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:43:52 Pharmaceutics Pharmaceutical sciences Clinical Data Management Pharmacology Pharmaceuticals policy Electronic Common Technical Document MUT Common Technical Document MedDRA Pharmaceutical industry Clinical research Research