Safety Monitoring in Clinical Trials

Monitoring patient safety during clinical trials is a critical component throughout the drug development life-cycle. Pharmaceutical sponsors must work proactively and collaboratively with all stakeholders to ensure a systematic approach to safety monitoring. The regulatory landscape has evolved with...

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Detalles Bibliográficos
Autores principales: Yao, Bin, Zhu, Li, Jiang, Qi, Xia, H. Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834937/
https://www.ncbi.nlm.nih.gov/pubmed/24300399
http://dx.doi.org/10.3390/pharmaceutics5010094

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3834937/
https://www.ncbi.nlm.nih.gov/pubmed/24300399
http://dx.doi.org/10.3390/pharmaceutics5010094

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