Exciting Updates: Enhancements to Our Platform!

October 1, 2024

Exciting Updates: Enhancements to Our Platform!

We are thrilled to share several key enhancements that will streamline your workflows and improve data management. 

Our Duplicates Search feature has received a significant upgrade! The system now identifies 100% duplicate files from your Inbox by checksum, ensuring cleaner data management. When files are moved from the Inbox to any folder in TMF Data, the system automatically searches for duplicates. If a match is found, users will receive a notification, allowing them to proceed or cancel the operation. 

This improvement makes file management smoother and reduces unnecessary duplicates in your TMF.

Refined AI Auto Classification Assistant

We’ve refined our AI Autoclassification Assistant to enhance your document management experience. This tool automates document classification, extracts key metadata, and delivers documents to the correct TMF location with greater precision. Benefits include fewer manual errors, improved data quality, and enhanced audit readiness. 

Your workflows will be more streamlined, fully aligned with the TMF Reference Model.

Enhancement in Subject Tracking and Invoicing

We are excited to introduce a new ‘Sync Procedures with EDC’ subsection in the Data Import section of our Subject Tracking module. This feature allows API consumers to synchronise procedure names between external EDC systems and our platform seamlessly.

Users can access all procedures included in budget documents, ensuring accurate data integration and improving efficiency in subject tracking.

Introducing Enhanced Virtual and Linked Files Feature

Our new Virtual and Linked Files functionality allows you to connect a single file for access across multiple studies. This feature significantly improves accessibility and flexibility, saving you time by eliminating the need to upload the same document multiple times. 

New API Endpoint for Enhanced Subject Tracking and Invoicing

We’re thrilled to announce a new API endpoint that allows you to post visit procedures data directly into the Subject Tracking and Invoicing module. 

This endpoint enables detailed and accurate posting of subject visits data at the procedure level and is available exclusively for projects using the ‘Per Procedure’ payment mode. It streamlines tracking processes and enhances project management capabilities.

These enhancements reflect our dedication to provide you with tools that enhance efficiency, accuracy, and compliance in your clinical trials management. Stay tuned for more updates as we continue to innovate and improve our platform!

Blog

June 25, 2026
The Quiet Revolution in TMF: How AI Document Classification Turns Routine into a Background Task

AI in Trial Master File management has quietly stopped being a someday idea. It’s not a pilot and it’s not a roadmap promise – it’s something clinical teams reach for on an ordinary Tuesday. The interesting part isn’t that AI can file a document; it’s how calmly and predictably it does it now – with […]

June 24, 2026
Investigator Site File Management with Flex Databases

Managing Investigator Site Files across multiple sites is one of the more operationally demanding aspects of clinical trial oversight. Flex Databases addresses this with a dedicated ISF module built around three distinct user experiences (Sponsor, CRA, and Site) each tailored to the workflows and priorities of its audience. The Sponsor View: Study-Wide Visibility Sponsors access […]

May 26, 2026
Looking for an Enterprise eClinical Solution? There Is More to Consider

When evaluating core clinical research platforms, most companies naturally start with the well-known enterprise brands. They are recognizable, widely adopted, and often positioned as the “safe choice” for regulated environments. But once the demo phase is over and implementation actually begins, many teams discover that choosing a platform involves much more than brand recognition and […]

May 21, 2026
Vendor Oversight Under ICH E6(R3): Why Compliance Expectations Are Higher Than Ever

Vendor oversight has always been part of clinical trial compliance, but ICH E6(R3) has significantly raised expectations for sponsors and technology vendors alike. The updated guideline makes one thing very clear: sponsors remain fully responsible for trial quality, patient safety, and data integrity — even when activities are outsourced to external vendors. This includes ensuring […]

Contact us

Get in touch to discuss compliance, implementation, demos, pricing

We are here for all of your questions! Tell us more about yourself and we will organize a tailored live demo to show how you can power up your clinical trials processes with Flex Databases.