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Clinical research / Drug discovery / Pharmacy / Clinical Data Management / Common Technical Document / Clinical pharmacology / Safety pharmacology / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Nonclinical studies / Pharmacology / Pharmaceutical sciences / Research


GUIDELINE FOR GOOD CLINICAL PRACTICE
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Document Date: 2012-06-22 05:07:25

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Company

ICH Expert Working Group / /

Country

Japan / United States / /

IndustryTerm

biotechnology-derived products / chemical form / pharmaceutical / drug product / chemical structure / human pharmaceutical / /

Organization

European Union / Steering Committee of Numbering and Section Headers / ORGANISATION OF MODULE / /

Position

Safety General / COMMON TECHNICAL DOCUMENT SUMMARIES General / General / /

Product

R1 / R2 / /

ProgrammingLanguage

DC / /

Technology

Pharmacokinetics / Pharmacodynamics / antibodies / biotechnology / /

URL

http /

SocialTag