Record Management

The TMF contains essential documents for a clinical trial which may be subject to regulatory agency oversight. Bearing this in mind, our Record Management team ensure a comprehensive, proactive and efficient approach to the design and operational maintenance of this key document repository.
The TMF can potentially contain thousands of documents and records requiring organisation and maintenance. Further complicating matter is the input from countless vendors, particularly in large, global studies. With Accelsiors systems and processes driving the management of key clinical trial documents you will experience real-time inspection readiness, visibility and control.
Our centralised Record Management team is dedicated to ensuring robust and proactive management of the study TMF. Their efforts are supported by our eTMF platform, Accelsiors Document Access Management system (ADAM), a web-based application to enable ready access to all study documentation. Electronic signature capability further increases productivity across the organisation. File structures are based on the TMF Reference Model, allowing direct access to support remote audit, inspection, and monitoring.
Feel free to ask Accelsiors’ Clinical Development experts!
Let’s start discussing about how we can support your pipeline! Please, contact us:
Write Us
Call Us: +36 1 299 0091
Request for Proposal
and we will schedule a meeting around your calendar!
WE ARE CONSCIOUS OF THE IMPORTANCE OF:
- Clear document management planning, especially during the critical start-up phase of a project
- Comprehensive team training
- Proactive document management and feedback
RECORD MANAGEMENT SERVICES:
- Record Management Plan development
- TMF/eTMF set up and maintenance
- Compliance reporting
Learn more about our comprehensive clinical development services
Accelsiors offers a complete range of expertise in support of your specific needs: Scientific, analytical and regulatory complemented by global resources, state-of-the-art technologies and project management methodology for the most effective execution of your development program across all phases of clinical drug development.

