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
- 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.