ArisGlobal

Understanding True eTMF Requirements – White Paper


Maximizing eTMF and eClinical Solutions for Improved Metrics and IRB Submissions
Given that eTMF solutions have been available for a while, why is the industry still struggling and why are inspectors still complaining and issuing critical findings because they can’t find the information they need? Compared to EDC, for example, the amount of fundamental discussion still ongoing indicates that the eTMF solutions are not working out as expected and overall process support is limited.

Download this white paper to understand the reasons for this failure and what benefits can be gained by unifying eTMF and eClinical solutions. You will learn how many of today’s eTMF solutions aren’t meeting the expectations of regulatory agencies and the industry and understand what a true eTMF requires in today’s complex, global trial environment.

Following the completion of a brief registration form, you can then access the white paper.

 

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