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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Br J Clin Pharmacol
Prif Awduron: Hoekman, Jarno, Klamer, Thea T., Mantel‐Teeuwisse, Aukje K., Leufkens, Hubert G. M., De Bruin, Marie L.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: John Wiley and Sons Inc. 2016
Pynciau:
Mynediad Ar-lein: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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