Clinical Trials Information System (CTIS): training programme

Clinical Trials Information System (CTIS): training programme

EMA has recently launched the CTIS training webpage for all user groups and organisations to facilitate their preparedness. This page contains information about the CTIS training programme and the online self-study material catalogue as foreseen by the CTIS training strategy.

The material available will gradually increase as the catalogue is complete module by module in batches. The positive feedback received on the materials has been greatly facilitated by the engagement of experts, including sponsor experts on CTIS and training, in the material production through consultation on learning objectives and validation of materials.

EMA’s training resources are tailored for clinical trial sponsors and staff of the European Union (EU) Member States, European Commission and other organisations who will use the system.

On April 26th from 10.00 to 11.30 am EUCROF Events&Training working group, chaired by Donato Bonifazi, is organising the webinar on the EMA Clinical Trials Information System.

In this webinar, Marieke Meulemans, CEO and Founder of GCP Central B.V., shows what training material has been created, where to find it and supports your preparation in the use of the CTIS with useful tips and considerations. Attending this webinar makes you aware of the steps to take in the next 9 months to get ready before the CTIS goes live in January 2022.

More information is available here.

2021-03-24T11:37:36+00:00 24/03/2021|Categories: News|