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Pharmaceutical sciences / Health / European Medicines Agency / Directive 2001/83/EC / Summary of Product Characteristics / Supplementary protection certificate / Qualified Person Responsible For Pharmacovigilance / Clinical research / Pharmaceuticals policy / Research


Draft COMMISSION REGULATION (EC) No …/.. of […] on the conditional marketing authorisation for medicinal products falling within the scope of Regulation (EC) No[removed]of the European Parliament and the Council of
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Document Date: 2013-10-09 09:24:03

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File Size: 27,91 KB

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City

Brussels / /

IndustryTerm

medicinal product / medicinal products / orphan medicinal products / /

MedicalCondition

seriously debilitating diseases / diseases / communicable diseases / /

Organization

World Health Organisation / COMMISSION OF THE EUROPEAN COMMUNITIES / Committee for Medicinal Products for Human Use / European Union / European Parliament / European Medicines Agency / /

Position

Official / EN General / /

ProgrammingLanguage

EC / /

PublishedMedium

the Official Journal of the European Union / /

SocialTag