Feasability study


  • We check thoroughly the feasibility of any kind of clinical trials.
  • We provide the feasibility questionnaire within the requested timeline.
  • We discuss the new studies with experienced Principal Investigators to ensure foreseen challenges are appropriately managed, and realistic numbers are provided.
  • We stand behind the numbers provided in feasibility, our recruitment team ensures enrolment numbers.

Clinical trial data entry

As a company dedicated to comprehensive planning and organization of clinical trials, we offer preparing documentation that is essential to conduct clinical research trials. Deep experience with digital patient diary, IWRS , eCRF etc.


  • Data is a key element of any clinical trial.
  • Appropriate data handling is critical in providing valuable and solid data.
  • Confidential handling of personal information according to GDPR and local data protection regulation

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Clinical study performance


  • Patient recruitment plan and performance
  • Data entry and data clarification
  • Handling study related documents and study medication
  • Site preparation for monitoring visits, authority inspection or audit
  • Pharmacovigilance reporting

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