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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


GUIDELINE FOR GOOD CLINICAL PRACTICE
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Document Date: 2012-06-22 05:07:22

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File Size: 286,45 KB

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City

Osaka / /

Company

ICH Expert Working Group / /

Continent

Europe / /

Country

Japan / United States / /

IndustryTerm

biotechnology-derived products / registration applications / pharmaceuticals / pharmaceutical / drug product / human pharmaceuticals / /

Organization

CTD Organisation / International Committee of Medical Journal Editors / FDA / Organisation of The Common Technical Document Diagrammatic Representation / Organization of the ICH CTD Common Technical Document Module / OF THE COMMON TECHNICAL DOCUMENT The Common Technical Document / Organisation of The Common Technical Document ANNEX / European Union / Organisation of The Common Technical Document GENERAL PRINCIPLES Throughout / Steering Committee of Numbering and Section Headers / Steering Committee of the Revision of the Annex / Organisation of The Common Technical Document Module / /

Product

R1 / M-16 / R2 / /

ProgrammingLanguage

DC / C / /

Technology

Pharmacokinetics / Quality of Service / biotechnology / /

URL

http /

SocialTag