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Regulating medicines in Europe: the European Medicines Agency, marketing authorisation, transparency and pharmacovigilance
Following a review process lasting almost four years, and culminating in several pieces of new European legislation, adjustments have been made to the European Union's (EU) regulatory framework for pharmaceuticals. The European Commission laid out its priorities for the review as: simplifying t...
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| Publicado no: | Clin Med (Lond) |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Royal College of Physicians
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4954442/ https://ncbi.nlm.nih.gov/pubmed/16521363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7861/clinmedicine.6-1-87 |
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