Flex Databases Application Release 10: What’s new

October 30, 2019

Flex Databases Application Release 10: What’s new

HR Database

Thank you for reading this post, don't forget to subscribe!
  • Ability to set up external users access and hide/unhide whole modules for different classes of users.

Investigators and Sites Management System

  • Ability to use free text format in site number.

CRA Activity Management

  • Offline capability: user now can fill in questionnaire offline and then upload it into the System
  • Connection to the Trial Master File: the system automatically uploads documents (Confirmation Letter, Monitoring Report, Follow-up letter, Additional documents) with the correct naming right to the necessary folder in Trial Master File. The system will create a new folder for each visit automatically. Files will be already in Locked status in TMF, so there is no need to go through QC process for the documents twice.
  • Configurable fields and trackers: user can now create any new trackers and fields in the system and add them to the Monitoring Visit workflow step. It’s possible to create several versions of a tracker.
  • Configurable templates: user can now customize the layout of the system generated documents (Confirmation Letter, Monitoring Report, Follow-up letter), to add user-defined trackers, fields, tables and digital signature(s).

Subject Tracking and Invoicing

  • Additional payment rules for Site payments: Complex Subject rule for custom subject payment, Holdback for open query for payment deduction in case of too many open queries, extra payment limitation.
  • Multi-currency: different currencies for budgets and for invoices for different beneficiaries. Users may either use fixed or live updated currency rates.

Trial Master File

  • Configurable QC Workflow: administrators are now able to define new steps of the QC Workflow in addition to the standard set of steps (Review-Approve-Lock). For example, you may add extra approvers to your flow.
  • Automatic upload and filing of documents via e-mail: user may now send files directly to a specified folder in TMF via e-mail. Administrators may restrict only authorized users to use this option.
  • Electronic Signature: user can now use User name/Password combination to confirm his approval/review of the document during the QC process.
  • Archiving: administrator can create an archive of the project documentation or an archive of the selected folders including with Audit Trail and Index report.

Reporting Tool

  • Users can now create any report (pivot, grid), set up rights on position, project or site level, set up graphs and diagrams, create reports, using data across modules or projects.

Blog

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. Thank you for reading this post, don’t forget to subscribe! 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 […]

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. Thank you for reading this post, don’t forget to subscribe! The updated guideline makes one thing very clear: sponsors remain fully responsible for trial quality, patient safety, and data integrity — even […]

Senior Project Manager | eClinical

We are looking for seasoned Senior Project Manager who is ready to take full ownership of high-impact projects. At our core, we value delivery over slides and results over rigid hierarchy.  Thank you for reading this post, don’t forget to subscribe! Our product is a SaaS eClinical platform designed for managing clinical trials and various business processes in the pharmaceutical […]

May 19, 2026
Clinical Trials Management Software: Key Features for CROs

CROs work in a fast-moving and highly complex environment. They manage multiple studies at the same time, often for different sponsors, across different countries, sites, and timelines. Each study comes with its own processes, reporting needs, and regulatory expectations. As this complexity grows, it becomes harder to keep everything aligned using separate tools or spreadsheets […]

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.

[ninja_form id=4]