Telemedicine Technologies Belgium offers Clinical Data Management services guaranteeing the highest quality of clinical trials data and outputs resulting from seamless Clinical Data Management services that are streamlined from protocol to clinical study report.
Telemedicine Technologies has been processing electronic data for the clinical research industry for over 2 decades, is ISO 9001 certified and is complying with applicable legislation like ICH GCP, GDPR and FDA 21 CFR part 11.
Its CleanWeb software is fully validated according to GAMP-5 guidelines ‘A Risk-Based Approach to Compliant GxP Computerized Systems’.
Added values provided by our experts:
- Vast experience in streamlined data collection and management
- Integrated Clinical Data Management services focused on quality of clinical trial data and outputs
- Telemedicine Technologies Belgium cumulates expertise covering all clinical trial phases
- Strong CDISC expertise
Added values provided by our own platform “CleanWeb”
CleanWeb is a secure e-Platform dedicated to the electronic management of ph. I-IV clinical trials, registries, observational studies and Managed Access Programmes.
CleanWeb is accessible either in SaaS mode or customised according to pharma, biotech, medTech industries and academia requirements.
- Autonomous solution
- Intuitive user interface
- Flexible design
- Interactive solution
- Real-time reports
- Personalised dashboards
- Simplified Data Management
- Dynamic IWRS
- Multilingual solution
- CDISC compliance
- SAS export
CleanWeb offers different modules:
- eCRF • ePRO/eCOA • IWRS • IMP Management
- Vigilance • Imaging • eTMF • CTMS • rSDV • MAP