• ICH GCP clinical research training (basic and experienced) for CRAs and site personnel (investigators, study coordinators, study nurses)
  • Standards and regulatory guidelines
  • Overall pre-study, monitoring and clinical management activities
  • (Serious) adverse event reporting and management
  • Professional and interpersonal skills and guidelines for Clinical Trial Personnel
  • Clinical Trial Agreements negotiation process
  • Legislation and compliance

We deliver high quality services 

in the Czech and Slovak Republics.

We put our emphasis on quality, experience, credibility and flexibility.

We invite you to consider our services and to contact us to discuss your clinical trial and pharmaceutical needs.