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Next Generation eClinical Applications

Introducing SureClinical, a collaborative cloud portal, best-in-class eClinical applications and platform designed to increase productivity, enhance quality and automate tasks in BioPharma clinical trials and Healthcare.

“With SureClinical eTMF Cloud, internal and external clinical study stakeholders can collaboratively complete, digitally sign and share regulatory and study information in the cloud from mobile or web. This strategic capability allows us to eliminate paper at point of origin, accelerating document completion and enhancing document quality.”

-Lynda Shelley, Executive Director of Clinical Operations, Novotech

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SureClinical eTMF

Manage, track and share clinical trial documents and medical images.

SureArchive

Global online access for completed studies with FDA and EC compliance validation.

SureClinical SNAP Platform

Gain a 360 degree view of your study with SureClinical’s Network Application Platform. Leverage existing applications and datasources in analytic dashboards in our next generation eClinical platform

Estimate cost savings with SureClinical eTMF

Clinical trial cost measurement has never been more important. The clinical trial master file (TMF) has traditionally been paper based, resulting in high labor costs and inefficiencies. This white paper shares operational details about how successful organizations are improving clinical operations ROI by automating TMF tasks.

Automate with Collaborative Clinical Trial Portals

Collaborative clinical trial portals can help improve operational efficiency, enhance quality and reduce time consuming manual processes in labor intensive clinical trials. Download this white paper to learn about the use of task automation, digital signing and collaborative tools for SureClinical's portal and eClinical applications platform.

Regulatory requirements and SureClinical

Adopt best practices to drive success with government regulatory requirements. Learn the details of how SureClinical meets government regulatory requirements FDA 21 CFR Part 11, European EC Annex 11, HIPAA and industry best practices through our global cloud, built in security policies, audit trails, and electronic signing policies.

Download - High Trust Digital Signing for Health Sciences

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Download - Evaluating Microsoft® SharePoint® based eTMF applications

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Download - Estimating TMF Costs

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Download - Cloud Compliance White Paper

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Download - SureClinical eTMF Flyer

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Download - Enhancing Clinical Trial Operations with Collaborative Cloud Portals

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