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Harmonisation
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#	Item
851	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
852	MEMOIRE DE LA CHAMBRE DE LA SECURITE FINANCIERE EN REPONSE A LA CONSULTATION RELATIVE A L’HARMONISATION DE LA REGLEMENTATION DU SECTEUR DE L’EPARGNE COLLECTIVE Add to Reading List Source URL: www.chambresf.com Language: French - Date: 2013-07-11 16:15:44
853	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
854	Guidance for Industry Submitting Marketing Applications According to the ICH-CTD Format — General Considerations DRAFT GUIDANCE This guidance document is being distributed for comment purposes only.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
855	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
856	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
857	REPORT OF THE ICH GLOBAL COOPERATION GROUP Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:43:46 Pharmaceuticals policy Pharmaceutics Research Pharmacology Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Quality by Design IFPMA MUT Pharmaceutical industry Pharmaceutical sciences Clinical research
858	Draft agenda of the GCG meeting 6 June 06 Yokohama Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:43:01 International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Needs assessment Research Clinical research Pharmaceuticals policy Drug safety
859	[removed]Federal Register / Vol. 77, No[removed]Monday, March 12, [removed]Notices ANNUAL BURDEN ESTIMATES Number of respondents Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-22 05:03:10 Pharmacology Clinical research Clinical pharmacology United States Public Health Service Regulatory requirement Unique Device Identification International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Food and Drug Administration Pharmaceutical sciences Pharmaceuticals policy
860	Microsoft Word - GCG132F_Final Report GCG_Meeting_Fukuoka_November 2010.docx Add to Reading List Source URL: www.ich.org Language: English - Date: 2012-06-21 12:44:23 Research Pharmaceutics Pharmaceuticals policy Pharmacology Drug safety International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use MedDRA EMBnet IFPMA Pharmaceutical industry Clinical research Pharmaceutical sciences