Training Programs

We offer a full range of training programs adapted to the specific needs of our clients:

  • 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.
  • Clinical Trial Audits and how to deal with auditors