Bluecompanion

We are a service provider specialised in the design, development, and implementation of Digital Platforms for Clinical Trials and Clinical Registries fully compliant with the highest regulatory standards.

CleanWeb® (Telemedicine Technologies, France) is at the core of our customised ICT systems. Each of our eCRF is uniquely designed according to the custom’s clinical trial protocol/clinical research project. Data from multiple sources are integrated: e.g., wearable connected devices (e.g., Withings), Patient Reported Outcomes (completed at home), data captured via robotic interfaces, via interactive conversational elements. Annexes can be recorded and accessed within the customised platform. Very different formats, e.g., row data from bio-imaging techniques, bioanalytical results’ tables, etc., can be uploaded to the system by the study personnel and appended to individual patients’ records. Structured data from legacy databases or federated environments can be read and integrated, as needed. 

Additional services include designing/writing the clinical protocol and related documents, medical monitoring and data management; and the e-Trial Master File. Bluecompanion Team has built wide experience in large international Consortia programs, in Academia driven clinical studies/registries and in biotech sponsored clinical trials.