Enhancing Clinical Trial Operations with Collaborative Cloud Portals
Clinical trials are burdened with mountains of paper and manual processes. The labor costs involved in the manual processes of collecting, uploading, tagging, classifying and tracking investigator documents are significant cost drivers in clinical trials. This white paper shows how leading BioPharma organizations are increasingly using collaborative cloud portals to capture, digitally sign and complete documents in the cloud through automated processes and tasks called workflows. Workflow task automation helps to eliminate paper at the point of origination, reducing or eliminating labor intensive document management processes. With automated workflows, clinical trial operations can realize significant cost and time savings over manual processes, while realizing higher levels of clinical trial data management quality, process compliance, reporting and auditability.
High Trust Digital Signing for Health Sciences
The traditional process of manually printing and signing a document is time consuming and starts a chain of labor intensive and error prone processes like scanning, uploading, tagging and QA.
Learn how organizations are eliminating paper at the point of origination and reducing the need for printing, scanning and uploading by using SureClinical’s patent-pending cloud and mobile digital signing solution. This article describes how SureClinical’s cloud-based digital signing capability can help your organization save money and accelerate document completion schedules and speeding the development of new drugs.
Evaluating Microsoft® SharePoint® based eTMF applications
A Comparison of Microsoft SharePoint based eTMF applications and Collaborative Cloud Portals in regulated health sciences applications
Cloud Compliance White Paper
Details of how SureClinical’s platform provides a compliance validated solution for clinical trial master file management under US FDA 21 CFR Part 11