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281	Friday, March 14, 2003 Part II Department of Add to Reading List Source URL: www.fda.gov Language: English - Date: 2003-03-14 06:29:13 Pharmaceutical sciences Clinical research Food and Drug Administration Drug safety Pharmaceutical industry Adverse Event Reporting System Postmarketing surveillance Pharmacovigilance MedDRA Medicine Health Pharmacology
282	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
283	ICH STEERING COMMITTEE November 9-10, 2011 Seville, Spain SUMMARY 1. Opening Discussions The ICH Steering Committee (SC) meeting in Seville was chaired by the EU. The Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:14 Drug safety Health Medicine Pharmacology Clinical Data Management Electronic Common Technical Document MedDRA Environmental Working Group EudraVigilance Clinical research Research Pharmaceuticals policy
284	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
285	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
286	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
287	Microsoft Word - ICH SC Meeting Yokohama Revised Summary clean.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:18 Research Medicine Medical informatics Pharmaceuticals policy Pharmaceutical industry Electronic Common Technical Document MedDRA Environmental Working Group Quality by Design Health Clinical research Pharmacology
288	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
289	Microsoft Word - ICH SC Meeting Portland-summary_without URL.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:13 Pharmacology Pharmaceutical industry Pharmaceutical sciences Health World Health Organization Electronic Common Technical Document MedDRA Environmental Working Group International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical research Research Pharmaceuticals policy
290	Microsoft Word - Summary_Yokohama_2007-clean.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 10:46:13 Research Health Pharmaceutical sciences Electronic Common Technical Document MedDRA Quality by Design Environmental Working Group Uppsala Monitoring Centre Regulatory requirement Clinical research Pharmacology Pharmaceuticals policy