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European Medicines Agency / Government / Pharmaceutical sciences / Directive 2001/83/EC / Qualified Person Responsible For Pharmacovigilance / Supplementary protection certificate / Clinical research / Pharmaceuticals policy / Research


Microsoft Word - EMEA comments on draft Regulation
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Document Date: 2013-10-09 09:07:11

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File Size: 204,36 KB

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City

Brussels / /

Company

Member States / /

Country

Belgium / /

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Event

Product Recall / Product Issues / /

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IndustryTerm

medicinal product / veterinary medicinal products / non-food producing target species / nicolas.rossignol@ec.europa.eu http /

Organization

COMMISSION OF THE EUROPEAN COMMUNITIES / EN EN COMMISSION OF THE EUROPEAN COMMUNITIES Brussels / European Parliament / European Medicines Agency / European Commission / /

Person

Nat / Nicolas Rossignol / /

Position

General / /

Product

periods / /

ProgrammingLanguage

EC / /

ProvinceOrState

Massachusetts / /

URL

http /

SocialTag