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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
Results: 311

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211	Draft Guidance Document - Preparatin of Drug Regulatory Activities in the Electronic Common Technical Document Format Add to Reading List Source URL: www.hc-sc.gc.ca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
212	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE Ref: GCG 65F GLOBAL COOPERATION GROUP MEETING REPORT Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:44:46 International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry MUT Association of Southeast Asian Nations Health Quality by Design Asia-Pacific Economic Cooperation Japan Pharmaceutical Manufacturers Association EMBnet Pharmaceuticals policy Clinical research Drug safety
213	18 July[removed]MEETING REPORT ICH Steering Committee June 5-6, 2013, La Hulpe, Brussels, Belgium Add to Reading List Source URL: www.ich.org Language: English - Date: 2013-10-14 04:55:44 Research Clinical Data Management Medical informatics Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA Electronic Common Technical Document La Hulpe Medicine Clinical research Health
214	REPORT OF THE ICH GLOBAL COOPERATION GROUP Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:44:33 Clinical research Science Pharmaceutical industry Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA MUT IFPMA Pharmacology Pharmaceutical sciences Research
215	INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE INFORMATION PAPER Step 3 Release E2B(R3) Add to Reading List Source URL: www.fda.gov Language: English Drug safety Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use IFPMA Pharmaceutical sciences Common Technical Document Standard operating procedure Clinical research Pharmaceutical industry Research
216	6 February[removed]MEETING REPORT ICH Steering Committee[removed]November 2013, Osaka, Japan Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-05-15 08:05:11 Pharmaceutical sciences Pharmacology Clinical Data Management Medicine Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA Electronic Common Technical Document Common Technical Document Clinical research Drug safety Research
217	E2B(R3) OID Information Paper Add to Reading List Source URL: www.fda.gov Language: English Universal identifiers Pharmaceutical industry Drug safety Pharmaceutical sciences Object identifier Medicine International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document IFPMA Identifiers Clinical research Research
218	Microsoft Word - GCG109F_Final_Report_of_GCG_Meeting_Yokohama_June_09.doc Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:44:44 Research Pharmaceutics Pharmacology Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document Good Clinical Practice Good manufacturing practice Clinical research Pharmaceutical industry Pharmaceutical sciences
219	Microsoft Word - 11175fnl_IG.docx Add to Reading List Source URL: www.fda.gov Language: English Research Pharmaceuticals policy Drug safety MedDRA International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Food and Drug Administration Specification Pharmacology Pharmaceutical sciences Clinical research
220	Appendix I (B) to the ICH E2B(R3) ICSRs Implementation Guide Backwards and Forwards Compatibility Add to Reading List Source URL: www.fda.gov Language: English Health Clinical research Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacovigilance Food and Drug Administration Email Pharmaceutical sciences Drug safety Pharmacology