We designed our Good Clinical Practice training programme to include International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use-standards and regulations, and tailored for local authority regulations.

We customize our training programs according to the audience. We offer the training programs for both young and for experienced clinical professionals. These services are both comprehensive and flexible, giving our clients the chance to learn and explore:

  • History of clinical trials
  • ICH-GCP introduction and structure
  • Principles of GCP
  • Importance of the consenting process
  • Ethics in clinical trials
  • Responsibilities of Investigators and Sponsors
  • Protocol compliance
  • Investigator brochure
  • Essential documents