Introduction to Good Clinical Practice (GCP)
This full day course is appropriate for all staff who are involved in any context with clinical research, in particular for those conducting a Clinical Trial for an Investigational Medicinal Product it is a regulatory requirement.
- History of Clinical Trials and the development of GCP
- Deciding what is a clinical trial
- Informed consent
- Responsibility of Research Personnel
This session is relevant to individuals who have no previous GCP training