In order to improve the quality of clinical trials of medicinal products, the Center regularly holds seminars on the topic “Good Clinical Practice (GCP). Regulatory framework for clinical trials in Ukraine”.
Among the issues covered by the Center’s specialists:
- Regulatory and legal framework for conducting clinical trials in Ukraine. Good Clinical Practice guidelines.
- Investigator responsibilities.
- Ethical aspects of clinical trials. Informed consent.
- Documents accompanying the clinical trial.
- Sponsor responsibilities. Monitoring. Audit.
- Clinical audit of a clinical trial.
Upon completion of the training seminars, participants are issued certificates. To participate, please fill out the application and send it electronically to: GCP@dec.gov.ua
We remind you that, along with webinars, the Center has established and is successfully implementing the practice of corporate GCP training in an online or offline format.
Application form for participation and cost of training at the link
