EMC Documentum Electronic Trial Master File SolutionSource: EMC Corporation
How Much Does A Missed Day To Market Cost Your Business?
Chances are, you're trying to control the skyrocketing costs of clinical trials by relying on contract research organizations (CROs) for the vast majority of your trials. But adding more resources—especially third parties—also adds enormous complexity to trial document management. The additional coordination required to collect and maintain vast numbers of trial documents from these partners can expose both you and the CRO to compliance risk. And the resulting delays in bringing a product to market are prohibitively expensive.
With the EMC Documentum Electronic Trial Master File (Documentum eTMF) solution, you can reduce this complexity and risk. Part of the EMC Documentum for Life Sciences solution suite, Documentum eTMF helps you centrally control and synchronize study artifacts, track progress in clinical trial documentation, and ensure fast, secure access to documentation both during and after trials. You'll realize gains in efficiency, consistently manage clinical trial documents according to Good Clinical Practices and ensure inspection-readiness.