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International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
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291	Microsoft Word - 9392fnl.doc Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Clinical research Pharmaceuticals policy Drug safety Therapeutics Center for Biologics Evaluation and Research International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacopoeia Medicine Health Pharmaceutical sciences
292	Federal Register / Vol. 64, No[removed]Friday, June 25, [removed]Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 97D–0444] Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Drug discovery Clinical research Pharmaceuticals policy Regulatory requirement International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Food and Drug Administration Drug development Pre-clinical development Pharmaceutical sciences Pharmacology Research
293	Guidance for Industry M4Q: The CTD-Quality August 2001 Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical industry Pharmacology Clinical Data Management Medical informatics Common Technical Document Food and Drug Administration International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Validation Package insert Clinical research Research Pharmaceutical sciences
294	Guidance for Industry M4: Organization of the CTD U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Add to Reading List Source URL: www.fda.gov Language: English Clinical Data Management Pharmacology Common Technical Document Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Electronic Common Technical Document Clinical trial Food and Drug Administration Research Clinical research Pharmaceutical sciences
295	GUIDELINE FOR GOOD CLINICAL PRACTICE Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:07:22 Science Electronic Common Technical Document Common Technical Document Pharmaceuticals policy International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical trial HTML element Documentation Clinical research Research Clinical Data Management
296	Pills over white background Add to Reading List Source URL: www.amrh.org Language: English - Date: 2013-11-04 02:31:06 Africa International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry East African Community Good manufacturing practice Food and Drug Administration Common Technical Document Regulatory requirement Pharmaceuticals policy Pharmaceutical sciences Pharmacology
297	EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL Consumer goods Pharmaceuticals PHARM 529 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:23:50 Medicine Health European Medicines Agency Directive 2001/83/EC Pharmacovigilance Medical device International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical Trials Directive Clinical research Pharmaceuticals policy Research
298	African Medicines Regulatory Harmonization Programme Stakeholder’s Plenary Consultation Thursday, 29th March[removed]Summary of Meeting and Add to Reading List Source URL: www.amrh.org Language: English - Date: 2012-07-17 04:31:36 Research Drug safety Pharmaceutical sciences Pharmacology International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical research Pharmaceuticals policy Pharmaceutical industry
299	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.amrh.org Language: English - Date: 2012-07-17 05:20:20 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
300	Microsoft PowerPoint - 11 FREISCHEM Barbara (IFAH).ppt [Mode de compatibilité] Add to Reading List Source URL: www.rr-africa.oie.int Language: English - Date: 2010-11-24 09:35:26 Medicine Occupations Regulatory affairs Research Health European Medicines Agency International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Clinical research Pharmaceuticals policy Pharmaceutical industry