Stakeholders’ views on the most and least helpful aspects of the ICH E6 GCP guideline and their aspirations for the revision of ICH E6(R2)

BACKGROUND: The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) has published the ICH E6(R2) Good Clinical Practice (GCP) guideline, which provides standards for the design, conduct, documentation, and reporting of clinical trials. Revision t...

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Detalles Bibliográficos
Autores principales: Dombeck, Carrie, Swezey, Teresa, Forrest, Annemarie, Tenaerts, Pamela, Corneli, Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468347/
https://www.ncbi.nlm.nih.gov/pubmed/36111176
http://dx.doi.org/10.1016/j.conctc.2022.100983

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468347/
https://www.ncbi.nlm.nih.gov/pubmed/36111176
http://dx.doi.org/10.1016/j.conctc.2022.100983

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