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.
- Introduction (History, Scope, Principles)
- Subject Protection (Ethics Committee, Informed Consent)
- Documentation (Protocol, Investigator Brochure, Source documents, Case Report Forms, Essential documents, Good Documentation Practices, Access)
- Safety Reporting
- 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 training@aml-research.be 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.