The “ICH-Good Clinical Practice (GCP) Training Course”, is an e-learning training course of around 3 hours aimed at providing a guide for all individuals that are involved in clinical research and clinical trials and they need to acquire GCP knowledge. The e-learning training course is based on the international E6 ICH Good Clinical Practice (R2), revised in 2016, and meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma, as necessary to enable mutual recognition of GCP training among trial sponsors. The ICH GCP training course is intended to provide indication for all the steps of a clinical trial, starting from the planning phase and Ethics Committee submission, passing through the trial conduction and up to the reporting of results.
Structure of the course
The course is available online on a dedicated e-learning platform (www.gcptraining.cvbf.net) and all materials can be viewed via web or saved by the user on the computer. The course is structured in 3 parts: an introductory presentation of the training course and 2 modules, each about one hour and a half. Each part is constituted by a PowerPoint presentation supported by audio comments.
Access to the course
To begin and access the course, the user should register himself/herself by filling in the registration form available at the “ACCESS TO THE COURSE” page to create his/her account. Once the user has already registered himself/herself and created the account, he/she can log in at the LOGIN page to access the course material.
Start the registration here!