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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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Bibliografske podrobnosti
izdano v:Br J Clin Pharmacol
Main Authors: Hoekman, Jarno, Klamer, Thea T., Mantel‐Teeuwisse, Aukje K., Leufkens, Hubert G. M., De Bruin, Marie L.
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2016
Teme:
Online dostop: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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