Our professional services

Main services

  • Project Management and Monitoring of clinical trials and non-interventional studies (NIS) according to Austrian Medicine Act (AMG) and Austrian Medical Devices Act (MPG)
  • Data capture, safety reporting and data management with a user-friendly eCRF-tool
  • Recruitment Services for accelerated and efficient patient recruitment
  • SUSAR-Reporting to the lead Ethics Committee and nominated investigational sites
  • Consulting and lectures: Training for investigators and clinical research associates including GCP, informed consent process, monitoring activities including coaching and start up training and mentoring, essential documents, SOP training
  • Conduct of Audits at investigational sites, at CROs or at the sponsor


We offer solutions tailored to the particular needs of your project, and we work together with you to determine a fee structure that is appropriate and transparent at all times.

Upon request, we can provide you with an all-inclusive solution which offers you the most in terms of predictability and security.