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ICH-GOOD CLINICAL PRACTICE (GCP) TRAINING COURSE



Consorzio per Valutazioni Biologiche e Farmacologiche (CVBF) is pleased to present the e-learning “ICH-Good Clinical Practice (GCP) Training Course”. 


The course is based on the international E6 ICH Good Clinical Practice (R2), revised in 2016, and is aimed at providing a guide for all individuals that are involved in clinical research and clinical trials and they need to acquire GCP knowledge.


This ICH E6 GCP Investigator Site Training 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.


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

  • understand the basics of Good Clinical Practice (GCP) and the current legal regulations and guidelines;
  • describe the main responsibilities of the involved parties;
  • get familiar with the essential trial-related documents (e.g. informed consent form, investigator’s brochure, protocol).



In this way, the participant will be aware of his/her role and responsibilities and will understand how GCP can be applied practically in the research setting.




Enjoy our educational activities!






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CVBF - Consorzio per Valutazioni Biologiche e Farmacologiche - Friday, 30 October 2020
Consorzio per Valutazioni Biologiche e Farmacologiche (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.    Privacy policy  -  Cookie policy