A regulatory binder is crucial for managing clinical trial documents, it ensures compliance with regulations, and makes audits easier. It helps keep important documents organized and readily accessible for trial monitors, auditors, and regulatory authorities, and serves as a useful reference for the research team. While it’s not legally required, maintaining a regulatory binder is […]
Even though electronic Trial Master File seems to be almost essential nowadays, there are still many questions on its value and benefits that it could bring to a company.
We’ve decided to answer the most common and most important of them and walk you through the entire process – from Why select eTMF through Legacy data migration to Smart eTMF, which works almost autonomously and takes care of your tomorrow.
Table of contents
Chapter 1: Why move to eTMF?
- What is eTMF?
- Integrating an eTMF system
Chapter 2: Paper TMF vs. eTMF?
Chapter 3: How eTMF saves money?
Chapter 4: What’s next for eTMF?
Chapter 5: How Flex Databases eTMF helps optimize clinical trial processes?
- Easy collaboration with the sites at no added cost
- How to move from paper to eTMF in three simple steps?
- On the way to the Neural eTMF
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