GCP Training

Good Clinical Practice Training

Our Good Clinical Practice (GCP) training curriculum includes International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) standards and regulations, and is customized for local authority regulations.

These custom in-person trainings are suitable for young and experienced clinical professionals involved in clinical trials worldwide. These services are both comprehensive and flexible, giving our clients the opportunity to learn and explore:

  • GCP indroduction and framework
  • GCP guiding principles
  • Informed consent
  • Ethical treatment of patients
  • Investigator responsibilities
  • Sponsor responsibilities
  • Clinical trial protocol
  • Investigator brochure
  • Essential documents