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SureClinical Announces SurePortal™, First 100% Paperless eTMF Investigator Portal for Automated Document Completion Across Mobile, Web
Date:10/31/2013

Rancho Cordova, California (PRWEB) October 31, 2013

To succeed in the increasingly regulated BioPharma clinical trial market, organizations need to ensure that clinical trial stakeholders can complete the growing mountain of regulatory documents efficiently, quickly, securely and cost effectively. Clinical trial study investigators, clinical research associates, clinical research organizations and employees need to access and complete documents digitally, in the context of the business process in which they are engaged. With conventional eTMF products or in-house solutions, users are relegated to cumbersome manual paper-based processes that are error prone, costly, and otherwise difficult to administer.
With SurePortal™, SureClinical addresses this challenge with the first 100% paperless Investigator Portal solution that runs on any web enabled mobile device for accelerated document completion.

With SurePortal, clinical trial managers can eliminate paper at the point of origination using SurePortal and SureWorkflow™ for paperless business process automation with integrated digital certificate signing. By helping BioPharma organizations enhance how they engage with information across all channels, the new SurePortal™ release for web, mobile and desktop accelerates clinical trial Investigator enrollment, improves productivity and business efficiency, and lowers document completion costs. Costly manual paper-based processes that involve printing, scanning, wet signing and overnight courier services can be replaced with automated workflow processes that support 100% digital document completion. By eliminating paper handling processes that are requ
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