Dear Colleagues,

This online GCP course is written by Dr Isaac John, Former Deputy Director of Research and Development at Ashford and St Peter’s Hospitals NHS Foundation Trust, UK and Professor of Health Sciences at Forman Christian University in Lahore, Pakistan. Dr John has many years of teaching and research experience.

The emphasis of the course is on removing all the legal jargon and presenting it in a simple form for clinical researchers to understand their responsibilities as laid out in the ICH-GCP guidelines and Country specific regulations. I welcome your feedback and comments to make sure that course is tailored to meet your expectations and requirements.

I hope you will enjoy this course, and you will have positive experience. Please do inform your colleagues and friends about this course and don’t forget the most important thing is to make sure that you put this knowledge into practice for the benefit and well-being of your patients and to deliver high quality clinical research.

Best wishes





Dr Isaac John
Hon Senior Lecturer
Royal Holloway – University of London
Deputy Director Research & Development
Ashford and St Peter’s Hospitals NHS Foundation Trust

WHO NEEDS THIS COURSE?
  • Trial Investigators
  • Trials Support Staff
  • Staff of Contract Research Organisations
  • Research Nurses
  • Staff of trial host organizations – R&D and administration
  • Ethics Committee Members
  • Junior Doctors aspiring to become Investigators
WHAT IS COVERED?
  • The Principles of ICH-GCP
  • Informed Consent
  • Ethics – IEC/IRB
  • Investigator Responsibilities
  • Sponsor Responsibilities
  • Trial Protocol
  • Investigator Brochure
  • Essential Documents
  • Safety Reporting
Assessment & Certificate
To qualify for a successful certificate you need to take our ICH-GCP Multiple Choice Exam which will assess your understanding of GCP guidelines and country specific regulations related to the course.

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