This short online, on-demand narrated or read-only course informs investigators and other site personnel about changes to GCP brought about by the ICH E6(R3) guideline.

It is aimed at those who already have current GCP training in place.

The course covers the new requirements that investigators need to adopt as part of their clinical trial practices.

What are the benefits of this sponsor training?
• Online, on demand. Do it anywhere! All that is needed is a strong continuous internet signal
• Globally log in at any time 24/7, 365 days a year
• Delivery by html 5 allows PC, laptop, iPad, iPhone and android mobile devices to be used
• Tracking of user activity, progress reporting  by user and group
• Certification for satisfactory completion
• The training is personalized using the participant’s first name
• The training is challenging and long enough to be a true training and evaluation option
• Costs depend on the number of participants with excellent packages for multiple users
• Fix costs with a 2-year agreement or longer
• Help in the event of problems
• Valuable e-resources in the course include a Guide to Consent, an Essential GCP book and a copy of the ICH GCP E6(R2) guidelines

For details of packages for training larger groups contact us at info@brookwood-global.com