The new CTIS (Clinical Trial Information System) information system harmonises and facilitates the evaluation and supervision processes for CTs (Clinical Trials). The course is designed to provide a general and practical overview of the most important aspects related to the implementation of the European CTIS Portal. This course presents the experience gained from its implementation to date in the use of CTIS from a practical perspective, both of the Sponsor (Sponsors) and the Ethics Committee (Authorities - CEIm).
- The course is structured into five live online sessions with an expert lecturer via the Teams platform, together with offline content available through the CBA FORMACIÓN Moodle platform.
- It will take place on 16, 18, 25, 27 and 30 September from 3:00 p.m. to 5:00 p.m.
- Aimed at staff working in clinical research, associated with REGIC (Network of Clinical Research Management Entities), and involved in the process of preparing and submitting documentation for the authorisation of clinical trials and their follow-up. It is also aimed at Study Coordinators, Regulatory Affairs staff, Project Managers and CTAs submissions.
info(ELIMINAR)@cbaformacion.com
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