QMENTA Platform 2.0

Latest release (September 2021)

This new version 2.0 includes several major improvements and new functionalities that are critical enablers of success in clinical research and clinical trial execution. 

This latest update includes:

Benefits:

  • Enable Audit Readiness. Users can easily demonstrate compliance with comprehensive and detailed audit trails capturing every event in data history, including document approvers, status changes, execution of a signature, authentication, and more. 
  • Improve GxP Quality and Compliance. We improved several features that help assure GCP compliance by the investigator and/or sponsor. LATER (read more and the link to the website page).
  • Improved customer support. The brain is complex enough, you don't need to spend time in IT and figuring out how to make things work. We are constantly improving the user experience and how to make the most of our products and services. We have worked on a new knowledge base; included a chat bot to help you quickly find answers; and as always, we are here to help.

Features:

  • Custom Electronic Signature and Manifestation. Approve data upload using electronic signatures and manifestations that are compliant with FDA Title 21 CFR Part 11 and Annex 11.

Screenshot 2021-09-08 at 17.36.45

  • Comprehensive Audit Trails. Easily demonstrate compliance with detailed audit trails capturing every event in data history, including document approvers and reviewers, status changes, execution of a signature, authentication, and more.

Screenshot 2021-09-08 at 17.47.14

  • Two-Factor Authentication (2FA). Besides having Password Security Policies for users to access and provide e-Signatures in QMENTA Platform, 2FA can be enabled requiring users to authenticate via SMS code.
  • Brand new unified login/registration experience for all QMENTA solutions.
  • General Fixes

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