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Design of experiments / Scientific method / Pharmacology / Pharmaceutical industry / Evaluation methods / Clinical trial / Placebo-controlled study / Placebo / Assay sensitivity / Clinical research / Research / Science


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 05:13:58

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File Size: 310,86 KB

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Company

ICH Expert Working Group / CONCURRENT CONTROL GROUP / /

Country

Japan / United States / /

IndustryTerm

control / /

MedicalCondition

pain / illness / depression / tumors / disease / /

Organization

European Union / /

Position

General / Investigator / Physician / blinded evaluator / Consolidated Guideline General / /

Technology

drug development / /

SocialTag