Collection of Data on Adverse Events Related to Medicinal Products: A Survey Among Registries in the ENCePP Resources Database

INTRODUCTION: As patient registries are not subject to regulatory requirements on the collection of adverse events (AEs) related to medicinal products, they may not have foreseen the collection of such information on a routine basis or as part of specific data collection schemes. OBJECTIVE: The Euro...

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Detalles Bibliográficos
Autores principales: Plueschke, Kelly, Jonker, Carla, Strassmann, Valerie, Kurz, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296377/
https://www.ncbi.nlm.nih.gov/pubmed/35729468
http://dx.doi.org/10.1007/s40264-022-01188-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9296377/
https://www.ncbi.nlm.nih.gov/pubmed/35729468
http://dx.doi.org/10.1007/s40264-022-01188-x

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