We offer a full range of training programs adapted to the specific needs of our customers:
- 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.