Data and document standards have existed for some time within the clinical trials arena and are considered essential for the identification, management, and exchange of clinical trial information between stakeholders and systems. These standards cover everything from clinical data collection to regulatory submissions. TMF is the final frontier when it comes to standardization, and standardization is still in its infancy. Having said that, there is a strong case for standardization and this presentation will explore that opportunity by drawing parallels with other areas of clinical trial conduct and discuss how we could take similar approaches to TMF and eTMF.
- Күн бұрын
TMF Week 2021 - Day 4 -11AM: Standardization of eTMF Drawing parallels in Industry
- Рет қаралды 21
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