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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
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191	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
192	[removed]Federal Register / Vol. 70, No[removed]Thursday, October 20, [removed]Notices FEDERAL RESERVE SYSTEM Formations of, Acquisitions by, and Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-10-20 09:12:56 Food and Drug Administration Pharmaceuticals policy Pharmacology Clinical research Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Regulatory requirement Center for Biologics Evaluation and Research Pharmaceutical industry Pharmaceutical sciences Medicine Health
193	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
194	ICH GCG ToR 09 November 2004 Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:41:03 Pharmaceuticals policy Pharmaceutical industry IFPMA EMBnet Research Pharmaceutical sciences Health Clinical research Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
195	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
196	Introduction to ICH INTRODUCTION TO ICH Add to Reading List Source URL: www.ich.org Language: English - Date: 2013-08-09 04:48:36 Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical Data Management Pharmacology Clinical research Research Pharmaceutical sciences
197	VALUE BENEFITS The Value and Benefits of ICH to Industry International Conference on Harmonisation of Technical Requirements for Registration of Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:41:17 Research Medicine Pharmaceuticals policy Pharmacology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Good Clinical Practice Clinical trial Regulatory requirement Good manufacturing practice Clinical research Pharmaceutical industry Pharmaceutical sciences
198	Guidance for Industry Submitting Marketing Applications According to the ICH-CTD Format — General Considerations DRAFT GUIDANCE This guidance document is being distributed for comment purposes only. Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Pharmaceutical industry Clinical Data Management Drug safety Common Technical Document New Drug Application International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Drug Master File Center for Biologics Evaluation and Research Clinical research Research Medicine
199	Annex 4: Q3C maintenance procedure  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 Clinical research Environmental Working Group Pharmacopoeia
200	Optimizing your eCTD ANDA Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Clinical Data Management Medical informatics Drug safety Electronic Common Technical Document International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Drug Master File Abbreviated New Drug Application Food and Drug Administration Clinical research Research Medicine