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Health / Pharmaceuticals policy / Pharmacology / Pharmaceutical industry / Food and Drug Administration / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Clinical trial / Methadone / Clinical research / Research / Chemistry


GUIDELINE FOR GOOD CLINICAL PRACTICE
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Document Date: 2012-06-22 05:11:45

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File Size: 209,97 KB

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Company

ICH Expert Working Group / /

Country

Japan / United States / /

IndustryTerm

likely degradation products / registration applications / on biotechnological/biological products / certain degradation products / degradation products / drug product / drug products / clinical trial applications / /

Organization

European Union / /

Position

representative / General / /

Product

R1 / R2 / /

ProgrammingLanguage

EC / C / /

SocialTag