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The UK BIO-TRAC Study: A Cross-Sectional Study of Product and Batch Traceability for Biologics in Clinical Practice and Electronic Adverse Drug Reaction Reporting in the UK

INTRODUCTION: Due to the complexity of biologics and the inherent challenges for manufacturing, it is important to know the specific brand name and batch number of suspected biologics in adverse drug reaction (ADR) reports. OBJECTIVE: The aim of this study was to assess the extent to which biologics...

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Detalhes bibliográficos
Publicado no:Drug Saf
Main Authors: Klein, Kevin, Hazell, Lorna, Stolk, Pieter, Shakir, Saad
Formato: Artigo
Idioma:Inglês
Publicado em: Springer International Publishing 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7048707/
https://ncbi.nlm.nih.gov/pubmed/31872358
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40264-019-00891-6
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