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Pharmaceutical industry / Clinical research / Pharmaceuticals policy / Food and Drug Administration / Quality / Validation / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Center for Biologics Evaluation and Research / Good manufacturing practice / Medicine / Health / Pharmaceutical sciences


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City

Rockville / /

Company

Expert Working Group / Pharmacopoeial Discussion Group / /

Country

Japan / United States / Canada / /

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Event

Reorganization / /

Facility

Rockville Pike / /

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IndustryTerm

delayed-release products / delayed-release/enteric coated products / manufacturing practice requirements / manufacturing practice / /

Organization

U. S. Department of Health and Human Services / Food and Drug Administration Center for Drug Evaluation and Research / Food and Drug Administration / office of Communication / U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research / European Union / ICH Steering Committee / Division of Drug / Dissolution Test General Chapter / Center for Biologics Evaluation and Research / Ministry of Health / Center for Biologics Evaluation and Research Food and Drug Administration / Information Center for Drug Evaluation / /

Person

Chapter Additional / /

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Position

A. General / V. A. General / /

ProvinceOrState

Maryland / /

URL

http /

SocialTag