GB Pharma has developed a digital platform for the management of clinical trials. Our eCRF platform allows the collection, management and reporting of data related to any kind of clinical study.
Our solution is extremely easy to use, fast and secure, and also includes eTMF and CTMS systems, which allow all clinical trial documentation to be collected within the same “repository”. In addition, thanks to the interconnection between the different modules, we are able to provide real-time statistics.
Validated in accordance with GAMP 5 guidelines and in compliance with FDA 21 CFR Part 11 requirements.
- e-CRF
- e-Monitoring
- e-Reporting
- Real time descriptive Statistic
- Export real-time Data
- Randomization and drug management for interventional studies
- e-Dictionary (for coding medDRA, ATC and other specific dictionaries)
- e-Pro
- e-TMF (Trial Master File)
- e-CTMS (Clinical Trial Master System)
- Increased compliance with procedures and improved patient engagement
- Decreased bureaucracy at sites and increased remote interaction
- Improved operational efficiency by providing robust data to facilitate internal decision making, enabling faster time-to-market