cvbf grt

CVBF is pleased to present the e-learning ICH-GOOD CLINICAL PRACTICE (GCP) TRAINING COURSE

Based on the international E6 ICHGCP (R2) revised in 2016 and aimed at providing a guide for all professionals involved in clinical research and clinical trials and that need to acquire GCP knowledge.

This E6 ICH-GCP Investigator Site Training meets the Minimum Criteria for the ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma, as needed to enable reciprocal recognition of GCP training among all the trial sponsors.

Upon completion of this online course you will be able to:

Understand the basics of GCP as well as current legal regulations and guidelines:

  • Describe the main responsibilities of each involved party
  • Get familiar with the essential trial-related documents (e.g. informed consent form, investigator’s brochure, protocols, etc.).
  • Participants will be aware of his/her role and duty, moreover they will understand how GCP can be practically applied in research settings.
Remember that the course must be renewed periodically to keep your certification up to date.

CVBF is a not-for-profit organisation, founded in 2000 with the mission to perform research and provide scientific, economic and regulatory consultancy for innovation in the health sector at European level. The main fields of interest are life sciences and biotechnologies, drug development for small populations (pediatric and rare diseases), research management and methodology, monitoring, statistics, regulatory, ethics and pharmacovigilance. Addressed to public bodies, research institutes and private companies, CVBF’s training activities support the Consortium’s areas of expertise.


Useful links