Aml Research

Fundamentals of ICH GCP E6 (R2) for Clinical Research Professionals

Major topics of the training:

The course is a comprehensive guide to the basic principles of ICH Good Clinical Practice aimed at any research professional active in clinical research. It reviews and demonstrates the principles of GCP. 

  1. Introduction (History, Scope, Principles)
  2. Subject Protection (Ethics Committee, Informed Consent)
  3. Documentation (Protocol, Investigator Brochure, Source documents, Case Report Forms, Essential documents, Good Documentation Practices, Access)
  4. Safety Reporting
  5. Relationship with other documents

Attendees will receive a training certificate and a pdf. of the course presentation


Who should take the course?

Participants do not need prior knowledge of ICH-GCP E6. The course is therefore relevant to any research professional active in clinical investigations.

For clinical research site staff we recommend the training: ICH E6 GCP (R2) training for Investigators and Site Personnel 


Duration: 120 minutes

Price: 185 € (Excluding VAT chargeable in Belgium and EU)

Course dates (Live webinar):

Thursday  September 16, 2021 at 14:00 CET

Tuesday October 05, 2021 at 20:00 CET

Other dates will be published shortly


Booking on to a course: 

If you want to register for this course, please send an email to and mention:

Course title
Course date
Title, First Name, Last Name and email addresses of trainees
Invoice details


Requests for registration should be send at least 3 days (72 hours) prior to the course date.

We will then provide you via email with a confirmation of registration and further information.

AML has the right to cancell the course if there are not more then 3 participants registered.