Immutep Selects Flex Databases eTMF to Improve Oversight and Compliance

March 10, 2026

Immutep Selects Flex Databases eTMF to Improve Oversight and Compliance

To learn more about the reasons behind this decision, we asked Tom Apelt, IT Manager at Immutep GmbH, to share his perspective on selecting Flex Databases and the experience of implementing the eTMF system.

Before implementing Flex Databases eTMF, what were the main challenges you experienced in TMF management?

Prior to implementing Flex Databases eTMF, our primary hurdle was the reliance on a legacy paper-based system. This created significant bottlenecks in two key areas: oversight and efficiency. With a physical TMF, we lacked real-time visibility into the status of our documents; we often didn’t know a document was missing or expired until we manually checked the binders, which made audit readiness a constant source of stress. 

What were the key criteria you evaluated when selecting an eTMF solution and vendor?

Our selection process focused primarily on two areas. First, we required Regulatory Compliance with eTMF filing regulations, ensuring the system maintained an immutable audit trail and inspection readiness (21 CFR Part 11 and DIA Model). Second, we evaluated the Total Cost of Ownership and Pricing, seeking a transparent model free of hidden fees for storage and long-term archiving to maintain financial predictability.

How would you describe your onboarding and implementation experience?

Overall, our onboarding experience with Flex Databases was positive, and we felt well-supported by the vendor team. However, we initially underestimated the scope of the implementation. The process of transitioning from our existing systems to FlexDB  was quite extensive, requiring significant internal time. Consequently, the acclimatization phase for our team to fully integrate the new system and its digital workflows into daily practice took longer than originally anticipated.

How has Flex Database eTMF improved efficiency, collaboration, and oversight across your studies?

Enhanced TMF Audit/QC check functionality significantly improved operational efficiency and improved direct and targeted communication regarding specific document corrections. Processes around document management, QC, and completeness checks are more streamlined.

How does the system help when working with external partners, such as CROs?

For a single project we gave access to certain members from a CRO. The system facilitates secure, controlled role-based access for CROs, establishing a basis for effective file sharing. This significantly improved sponsor oversight into CRO activities.

What advice would you give to other sponsors evaluating eTMF solutions?

We would recommend to prioritize scalability and seamless TMF Reference Model implementation. Ensure robust access right management (even at the folder level), comprehensive audit trail availability, and validated documentation. Robust export functionality is also critical for regulatory requirements and transfers.

Blog

April 15, 2026
TMF Blinding: Removing the Complexity of Managing Blinded Studies

Blinded studies are critical for maintaining the integrity of clinical trials. But while the concept is straightforward, the operational reality is often anything but. For many clinical teams, managing blinding means dealing with: This creates a constant burden: Even with strict processes in place, a single misconfiguration can compromise the entire study. TMF Blinding in […]

April 2, 2026
CTMS for CRO Financial Management: Managing Clinical Trial Budgets and Investigator Payments

Financial management is critical because CROs must ensure that clinical trials remain within budget while generating expected revenue. Without proper financial oversight, organizations may experience delayed payments, incorrect invoicing, or reduced project profitability. A CTMS helps CROs maintain financial control and improve operational efficiency. Financial management is one of the most complex operational areas for […]

April 1, 2026
Risk-Based Monitoring (RBM) in Clinical Trials: A Comprehensive Guide to Modern Oversight

For decades, the clinical research industry operated under a manual, labor-intensive oversight model. The gold standard was 100% Source Data Verification (SDV) – a process where Clinical Research Associates (CRAs) traveled to sites to painstakingly cross-reference every data point in a Case Report Form against medical records. However, as trials have become more data-saturated and […]

March 26, 2026
Why MapLight Therapeutics Chose Flex Databases’ CTMS and eTMF

MapLight Therapeutics selected Flex Databases to support its clinical trial operations with an integrated CTMS and eTMF platform. In this interview, the MapLight team shares why they chose Flex Databases, which features stood out during the evaluation process, and how the platform will support efficient trial oversight and long-term clinical operations. What were the key […]

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.