+49 6187 905 91 47 sales@medsurv.de

MedSurv

practice-proven. modular.
innovative.

MedSurv

practice-proven.
modular.
innovative.

The MedSurv-Portal

Who we are

With the MedSurv portal, we provide our customers with an online EDC system for data collection in:

  • Clinical studies
  • Non-interventional studies (NIS)
  • Patient registry
  • Post-marketing observational studies
  • PMCF studies

How we work

We assist our customers all along their way – from their planning of the eCRF to the validation of the system. We also ensure that all project steps are undertaken in a well-structured sequence.

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 further.

Who we are

With the MedSurv portal, we provide our customers with an online EDC system for data collection in

  • Clinical studies
  • Non-interventional studies (NIS)
  • Patient registry
  • Post-marketing observational studies
  • PMCF studies

How we work

We assist our customers all along their way – from their planning of the eCRF to the validation of the system. We also ensure that all project steps are undertaken in a well-structured sequence.

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 further.

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

U

Audit Trail

Tracking of changes according to legal requirements

Randomisation

Customisable algorithm
Reliable ratio

 

q

(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

i

Query Management

Direct communication in the portal

Patient access

Direct collection of questionnaires (QoL)
Patient diary

n

Document upload

Uploading of documents with patient allocation

Clinical Trial Management

Daily updates of study data
Transparency
Remuneration
Recruitment status…

 

 

News

Testimonials

Testimonials

Where to find us