Site Data Management

It seems to you that during clinical trials you spend more time on administration than with patients / clinical trial subjects?

We have a solution for you, which will reduce the administrative burden on you and your entire team of up to 40%!

Use the services of Site Data Manager which for you:

  • enters data from source documents into CRF / eCRF
  • resolved:
    • Unclarity in the source documentation related to entering data into the eCRF / CRF
    • Answers to Data Query / Data Clarification Forms
    • Questions in the SAE Responses to laboratory results

For more information you can contact us via the contact form.

 

Feedback