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Pharmaceutical industry / Pharmaceuticals policy / Marketing authorization / Qualified Person for Pharmacovigilance / Homeopathy / Supplementary protection certificate / European Directive on Traditional Herbal Medicinal Products / Medicine / Pharmaceutical sciences / Health


EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL
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Document Date: 2014-03-17 12:34:52

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File Size: 188,00 KB

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City

Bruxelles / /

Company

Module 1 Manufacturing / /

Country

Norway / Belgium / Iceland / /

Event

Reorganization / /

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IndustryTerm

manufacturing authorisation holders / pharmaceutical form / medicinal product / homeopathic stock manufacturer / manufacturing sites / authorised medicinal product / manufacturing / manufacturing site / manufacturing practice / pharmaceutical form change / homeopathic medicinal product / authorisation/registration applications / finished homeopathic medicinal product / manufacturing authorisation / biotechnology change / active substance manufacturer / prescription* product / manufacturing process / manufacturing authorisations / /

Organization

EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE / Council of Europe / EUROPEAN COMMISSION / /

Person

Volume / /

/

ProgrammingLanguage

EC / /

Technology

pharmacokinetics / biotechnology / /

SocialTag