You need to update and to refresh your knowledge on the current ICH-GCP E6 (2) and its implementation and you want to do it in a very practical and useful way? Then this eLearning course is designed for you.
How is this course different from other GCP refreshers? It is conducted in a very interactive way to review ICH-GCP through workshops, quizzes and several real-life situations.
Documents and materials related to this course are included
Globally recognised certificates awarded after test completion
This course has been granted PharmaTrain Recognition
Course credit: 4h (3 months period to complete course)
Complete the course at anytime, anywhere!
This interactive eLearning course is designed for professionals who already have knowledge of the International Council on Harmonization and Good Clinical Practice (ICH-GCP) standard but need to be up-to-date. It is designed as a refresher and will cover the responsibilities of all players in the clinical research field. This refresher session is a very innovative course which will allow you to verify the extend of your knowledge on ICH-GCP and complete the potential gap.
Interactive quizzes and exercises are included in our eLearning course that give you immediate feedback on your comprehension. This will help you to maximise your learning journey. You will be able to test your comprehension with a final grading test. Extra information, updates and your Transcelerate globally recognised certification can be found on our Virtual Campus.
Refresh your knowledge on current GCP requirements in clinical research and how they are implemented
Interpret the essential documents of clinical studies
Grasp what GCP implies for you in your daily work
Obtain a clear view on the items added by the Addendum 2016
Learn how to avoid findings in case of audit and/or inspection
Refreshing Definitions and Principles of GCP
Responsibilities for all involved persons/parties
The essential GCP-related documents
Impact of the 2016 GCP addendum for Investigators and for Sponsors
GCP Audit Findings at the Sponsor and at the Investigational Sites
Who should attend
Everyone who needs to refresh their knowledge of the current rules of GCP in clinical studies. Prior training or working experience in a GCP environment is required.
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