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European Union pharmacovigilance capabilities: potential for the new legislation
European Directives and Regulations introduced between late 2010 and 2012 have substantially overhauled pharmacovigilance processes across the European Union (EU). In this review, the implementation of the pharmacovigilance legislative framework by EU regulators is examined with the aim of mapping D...
Uloženo v:
| Vydáno v: | Ther Adv Drug Saf |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
SAGE Publications
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4530350/ https://ncbi.nlm.nih.gov/pubmed/26301067 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2042098615591802 |
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