- Design & deliver clinical research training for you, either in the classroom or online.
- Help your clinical research trainers develop and deliver their own material.
- Review and validate your existing clinical research training material.
We have experience designing and delivering training in the following subjects:
- ICH GCP
- Monitoring, including Risk Based Monitoring
- Sponsor Responsibilities
- Investigator and site staff responsibilities
- Inspection readiness
- 21 CFR and FDA guidance
- EU Clinical Trials legislation and guidance
- UK Clinical Trials legislation and guidance
- GMP for IMPs
- ISO14155 (GCP for Medical Devices)