Maxer delivers the CTIS training program for Dompé
On 28 and 29 June, Erika Ornago and Massimo Zaninelli (Maxer Consulting) performed for Dompé S.p.A. the “Working with CTIS” training programme, which focuses on the EMA clinical trial information system. The Clinical Operations and Regulatory Affairs teams of Dompé participated in the two sessions. The participants fueled a lively debate on critical issues regarding the functionalities and requirements of the CTIS, the transition period, and the transparency rules envisaged by Regulation 536/2014.
The training provided by the Maxer team is based on the contents of the EMA CTIS Master Trainer Program. The first session provided a broad overview of CTIS features providing suggestions on how to work within the platform. The main objective of the second session was to illustrate the operational information to the sponsor for working with the Clinical Trial Information System (CTIS) platform.
This Maxer Consulting CTIS training programme is available in both English and Italian. Suppose you are a clinical research sponsor and are interested in better understanding the new features of the CTIS portal. In that case, you can find more information about the training on our website www.maxerconsulting.it or please feel free to email us anytime at info@maxerconsulting.com
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