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Characteristics and follow‐up of postmarketing studies of conditionally authorized medicines in the EU

AIM: The aim of the present study was to provide an insight into the characteristics and follow‐up of postmarketing studies of medicines that were conditionally authorized in the European Union (EU). METHODS: We compiled a list of all postmarketing studies attached as specific obligations to the lic...

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書目詳細資料
發表在:Br J Clin Pharmacol
Main Authors: Hoekman, Jarno, Klamer, Thea T., Mantel‐Teeuwisse, Aukje K., Leufkens, Hubert G. M., De Bruin, Marie L.
格式: Artigo
語言:Inglês
出版: John Wiley and Sons Inc. 2016
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4917806/
https://ncbi.nlm.nih.gov/pubmed/26992001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bcp.12940
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