GCP and clinical operations
- ICH GCP E6(R3) for CRAs, CRA candidates, Investigators and site teams
- Clinical trial monitoring
- Study start-up and clinical trial regulations
- Audit and inspection readiness
Trainings
Training portfolio
Practical learning for clinical research teams
Brillance combines current regulatory requirements with practical examples, exercises and discussion based on the realities of clinical trial delivery.
Our training portfolio
Established modules for clinical operations professionals, Investigators and site teams.
Investigators and site teams
- Study Nurse in Clinical Trials
- Roles, responsibilities and site readiness
- Essential documentation and source data principles
- Communication and conflict resolution
Specialized capability
- IATA-compliant transport of biological samples
- Structured programs for institutions and site networks
- Selection of established modules for the relevant professional audience
Current standards
Programs reflect current requirements and role-specific responsibilities.
Practice-led learning
Realistic examples, exercises and case-based discussion support practical application.
Documented completion
Each completed training module concludes with a certificate of attendance.
Discuss training support for your team
Tell us about the professional audience and the capability area you would like to develop.
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