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Harmonisation
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661	[removed]Federal Register / Vol. 65, No[removed]Thursday, May 4, [removed]Notices Management Branch, Procurement and Grants Office, Centers for Disease Add to Reading List Source URL: www.fda.gov Language: English - Date: 2000-05-04 05:29:31 Pharmaceuticals policy Pharmaceutical industry Common Technical Document Regulatory requirement Food and Drug Administration IFPMA Nuisance Pharmaceutical Research and Manufacturers of America International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical sciences clinical research Pharmacology
662	Co-ordination & Harmonisation of Advanced e-Infrastructures for Research and Education Data Sharing A CHAIN-REDS solution for accessing computational services Rafael Mayo García, CIEMAT Add to Reading List Source URL: tical2014.redclara.net Language: English - Date: 2014-06-17 09:10:32 CESNET Centre for Development of Advanced Computing IHEP Astronomy Universe Orion constellation Greek Research and Technology Network Sigma Orionis
663	PRESS RELEASE Invitation to Submit an Expression of Interest for the MSSO Tender Geneva, February 10, 2014 – The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals f Add to Reading List Source URL: www.ich.org Language: English - Date: 2014-02-10 03:59:08 MedDRA Drug safety Research Pharmaceutical sciences International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmaceutical industry Science Clinical research Pharmacology Pharmaceuticals policy
664	PSC INTOSAI Professional Standards Committee Drafting conventions for Auditing Guidelines Introduction These drafting conventions were developed by the ISSAI Harmonisation Project in consultation with Add to Reading List Source URL: www.issai.org Language: English - Date: 2014-06-11 07:48:46 Business International Standards on Auditing Audit Financial audit Materiality Performance audit International Organization of Supreme Audit Institutions Auditor independence Auditing Accountancy Risk
665	LAYMAN’S REPORT WEEELABEX LIFE07 ENV/B[removed]Harmonisation of a common set of European standards for the Add to Reading List Source URL: www.weee-forum.org Language: English - Date: 2014-10-23 16:16:58 Electronic waste Waste management Law Waste Electrical and Electronic Equipment Directive Extended producer responsibility Audit Computer recycling Electronic waste by country Waste legislation European Union directives Environment
666	The Evolution of ICH Shift From Input to Output-The Influence of the CTD Justina A. Molzon, MS Pharm, JD Associate Director for International Programs Center for Drug Evaluation and Research US Food and Drug Administrati Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:06:30 Clinical research Clinical Data Management Pharmaceutical industry Electronic Common Technical Document MedDRA IFPMA Food and Drug Administration International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Common Technical Document Pharmaceutical sciences Research Pharmacology
667	Bijuridisme et harmonisation : Genèse Add to Reading List Source URL: www.canada.justice.gc.ca Language: French - Date: 2013-04-30 14:47:39
668	Microsoft PowerPoint - _Special - Morin - ICH [Compatibility Mode] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:08:38 Pharmaceutical industry Health Pharmaceuticals policy Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Pharmacology Japan Pharmaceutical Manufacturers Association Clinical trial IFPMA Clinical research Research Pharmaceutical sciences
669	Microsoft PowerPoint - 5) Pharmacopeia_SK.ppt [Compatibility Mode] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:05:51 European Directorate for the Quality of Medicines Strasbourg European Pharmacopoeia Medicine Europe Pharmaceuticals policy Health International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use European Union Council of Europe Pharmacopoeias Homeopathy
670	Microsoft PowerPoint - Breakout B CS Summary.ppt [Compatibility Mode] Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 04:05:50 Pharmaceuticals policy Association of Southeast Asian Nations Clinical research Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use

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