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eCRF / ePRO
practice-proven.
modular.
innovative.
The MedSurv-Portal
Who we are
We provide our customers an validated online EDC system (eCRF/ ePRO) for data capture in:
  • Clinical studies
  • Non-interventional studies (NIS)
  • Patient registry
  • Post-marketing observational studies
  • PMCF studies
How we work
We accompany our customers from the planning of the eCRF to the validation of the study-specific requirements and ensure a structured project workflow.
On request, we can offer a full service with reliable and internationally active partners, such as CROs, data managers, statisticians, biometrists, etc.
What makes us
We offer our costumers
  • Strong project management
  • Fast response times
  • Sustainability
  • Direct and personal support
Our quality results from our certified management system. We are constantly developing ourselves and our user-friendly tools.
Compliance
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Modules
Audit Trail

Tracking of changes according to legal requirements

Randomisation

Customisable algorithm

Reliable ratio

(S)AE Management

(Serious) adverse events are automatically processed)

Monitoring

Virtual data check

Current patient and visit status

Management of the centres

Data Management

Additional validation process according to DVP

Query Management

Direct communication in the portal

ePRO/ eDiary

Direct collection of questionnaires (QoL)

Patient diary

Document upload

Uploading of documents with patient allocation

Clinical Trial Management

Daily updates of study data

Transparency

Remuneration

Recruitment status…

Testimonials