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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
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