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Clinical trial master file migration: A preordained step for a centralized electronic trial master file
The need to speed up clinical trial processes in a cost-effective manner, increased importance of data integrity, and ensuring timely compliance to regulatory requirement updates regarding the Trial Master File (TMF), has made the pharmaceutical industry delineate the requirement to maintain a centr...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Wolters Kluwer - Medknow
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7819366/ https://www.ncbi.nlm.nih.gov/pubmed/33489830 http://dx.doi.org/10.4103/picr.PICR_106_19 |