Managed EDC and Statistical Services Services for Research Studies
EDC, automated TFLs and automated analysis in one platform
From eCRF programming and validation checks to dashboards, conditional notifications and final data delivery, our team handles the technical database work so your researchers can concentrate on running the study.
We work with CROs, research organisations, universities, healthcare teams, medical-device companies and other organisations that need a dependable data-capture system without keeping an internal programming team.
| ID | Site | Follow-up |
|---|---|---|
RG-1281 | 02 | 12 m done |
RG-1282 | 05 | 6 m due |
RG-1283 | 01 | Baseline |
RG-1284 | 03 | New |
Trusted and used by leading pharmaceutical companies
Eight study types we support:
We translate your approved questionnaire, protocol requirements and data specifications into a study-ready electronic Case Report Form.
Your database can support
We configure databases for multiple study visits, repeated assessments, participant follow-up and long-term outcome monitoring.
Depending on your study, the database can include
Registries can be configured for one or more conditions, sites, treatment pathways or patient groups, with user roles and permissions set according to each organisation's responsibilities.
Registry functionality can include
We support post-market surveillance studies for medical devices, healthcare products, digital-health technologies and other regulated or evidence-led products.
Data-capture workflows can cover
We support studies that need repeated data collection, participant segmentation and detailed analysis of actions, experiences and outcomes.
A study can include
Participants complete questionnaires on a computer, tablet or mobile device, so outcomes and experiences are recorded closer to the time they happen.
We can configure
We configure multilingual questionnaires while keeping variable names, response codes and data outputs consistent across every language version.
Projects can include







