Trainings
Training & Workshops
We deliver practical, role-based training for clinical research professionals and site teams - online or on-site - tailored to your study, organization, and compliance requirements.
CRA & Clinical Operations
- ICH GCP R3 (for CRAs and CRA candidates)
- Clinical Trial Monitoring (workshop-based, case studies)
- Clinical Trial Start-up / Study Set-up
- Audits & Inspections readiness (CRO / site perspective)
- Clinical trial regulations (national & international - high-level overview)
Investigators & Site Teams
- ICH GCP R3 (for Investigators and study team members)
- Study Nurse in clinical trials (practical course)
- Site readiness: roles & responsibilities, documentation & source data basics
- Team communication and conflict resolution in the site environment
- Audit/inspection preparedness and follow-up basics
Specialized Modules
- IATA-compliant transport of biological samples (role-focused training)
- Tailored workshops for site networks and clinical trial support centers (on request)
Trainings Department – contact
For enquiries, please contact us at: training@brillance.pl.
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Each training module concludes with a certificate of attendance. Detailed agendas and pricing are provided upon request.