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As a Ph.D. student or a researcher at a university, you can benefit from managing your clinical trials professionally and save time by organising and automating your collection of data.


GDPR offers you safe collection and storage of personal data and complies with the GDPR. adheres to the strict legislation, GDPR, and regulations of the handling of personal data, and has been security approved by several European universities. is an online CMTS that enables you to carry out all operational and logistical tasks in one system.

  • Design of surveys

  • Consent forms and online signature

  • Distribution by secure email

  • Automatic reminders to participants

  • Booking system for visits

  • eCRF creator

  • Data storage in GDPR-compliant online system

  • Granting of access to data to stakeholders all over the world

  • Real-time data

  • Easy reporting

  • Analysis of data in secure system through integration to statistical applications

Randomisation of participants

The system is able to randomise participants automatically so that each participant has an equal chance to be assigned to any group that you have set up in your clinical trial. Sample sizes are set by you directly in the system.

Randomisation prevents selection and accidental bias.


All phases of any clinical trial can be carried out in – and you can get a free trial and demo any time before you make up your mind.

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Key Features
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