+49 6187 905 91 47 sales@medsurv.de

eCRF / ePRO

practice-proven. modular.
innovative.

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.

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

CDISC

US FDA
21 CFR
Part 11

EU GxP
Annex 11

FDA Industry
Guidelines

ICH-GCP
Guidelines

CDISC

US FDA
21 CFR
Part 11

EU GxP
Annex 11

FDA Industry
Guidelines

ICH-GCP
Guidelines

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…

 

 

News

Testimonials

Testimonials