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Clinical research / Medicine / Pharmaceuticals policy / Drug safety / Pharmaceutical industry / Pharmacovigilance / Adverse effect / Regulatory requirement / Adverse event / Pharmacology / Pharmaceutical sciences / Health


INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE
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Document Date: 2012-06-22 05:13:28

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File Size: 212,57 KB

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Company

AEs / ICH Expert Working Group / /

Country

Japan / United States / /

IndustryTerm

chemical entities / medicinal products / manufacturing process / /

MedicalCondition

renal disorders / disease severity / /

Organization

World Health Organization / European Union / /

Position

General / /

Technology

biotechnology / /

SocialTag