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


EN Official Journal of the European Union
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Document Date: 2013-10-09 08:55:57

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File Size: 97,95 KB

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Company

Member States / /

Event

Product Issues / Product Recall / /

IndustryTerm

homeopathic and traditional herbal medicinal products / medicinal product / veterinary medicinal products / authorisation applications / medicinal products / coordination / /

Organization

World Health Organisation / Standing Committee on Veterinary Medicinal Products / EC OR CHAPTER / European Medicines Agency / Standing Committee on Medicinal Products for Human Use / COMMISSION OF THE EUROPEAN COMMUNITIES / European Union / European Parliament / /

Position

author / EN Official / /

Product

periods / /

ProgrammingLanguage

L / EC / /

ProvinceOrState

Iowa / /

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