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Health / Clinical Data Management / Medical informatics / Pharmaceuticals policy / Pharmaceutical industry / Electronic Common Technical Document / Common Technical Document / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Marketing authorization / Clinical research / Medicine / Research


CTD General Q&As June[removed]
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Document Date: 2012-06-22 05:07:22

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File Size: 77,11 KB

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City

Osaka / /

Company

AEs / /

Country

Japan / United States / /

/

Facility

Hospital Re-admission / /

IndustryTerm

admin@ich.org Web site / to generic drug applications / /

Organization

Organisation of the CTD / Organisation of the Common Technical Document / European Union / ICH Secretariat / ICH Steering Committee / Steering Committee / Steering Committee of Numbering and Section Headers / Steering Committee of the Revision of the Annex / European Commission / /

Person

Louis-Dunant / /

/

Position

General / CTD General / /

Product

R1 / M-16 / R2 / /

ProvinceOrState

New Brunswick / /

Technology

DTD / PDF / /

URL

http /

SocialTag