Virtual “Introduction to Clinical Research & GCP"             
Contact us for upcoming course dates

• This course will be delivered in two x 2-hour webinars.
• A PDF course book will be provided. Participants should print the course book in advance – this will be used during the course to undertake individual tasks.
• The course will consist of presentations, poll questions, interactive tasks and discussion, and followed by an online quiz.

Session 1
• Introduction to course
• Phases of research and common trial designs and terminology.
• What is GCP and who does it apply to?
• GCP principles.
• Study protocol and compliance
• The critical path of the clinical trial.

Session 2

• Session 1 recap
• Investigator site and suitability.
• How patients are protected in clinical trials :Helsinki, consent and ethics.
• Investigational Medicinal Product (IMP).
• Safety reporting.
• Data collection, reporting and quality.
• Document generation: content and management of the Trial Master File.
• Audits and inspections explained

The content of each session is a guide only. Topics may be switched between sessions to provide participants with the best learning experience but overall content will remain the same.

'It has been a pleasure to attend such an excellent course. I really enjoyed it and learnt many relevant information about methodology and terminology in Clinical Research.

Please extend my thanks to Prof Dr David Hutchinson and Dr Colin Wilsher, they are excellent speakers!

Thank you again for the great course, I would certainly recommend it and I hope to be able to attend other courses in the future.' - ET

It was one of the most interesting, good, useful and nice trainings which I ever had! Thank you! -  KP J&J