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Pharmaceutical sciences / Pharmacology / Health / Food and Drug Administration / Drug safety / Clinical trial / Investigational New Drug / Drug development / Pharmacovigilance / Clinical research / Pharmaceutical industry / Research


INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE ICH HARMONISED TRIPARTITE GUIDELINE DEVELOPMENT SAFETY UPDATE REPORT
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Document Date: 2012-06-22 05:14:06

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File Size: 334,39 KB

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City

Geneva / /

Company

ICH Expert Working Group / /

Country

Japan / United States / /

Event

FDA Phase / /

IndustryTerm

experimental product / fixed combination product / medicinal products / manufacturing process / /

MedicalTreatment

multidrug therapies / drug therapy / /

Organization

European Union / Steering Committee / /

Position

DSUR Executive / Reference Safety Information The Investigator / Page Executive / E8 General / /

Product

Investigational Drug / MEDIA436 / /

RadioStation

8 When / /

Technology

drug development / /

URL

http /

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