Clinical Trials Information System (CTIS) bitesize talk: User access and role management

Date: 24/02/2022
Location: Online, 14:00 - 15:30 Amsterdam time (CET)

Event summary

This bitesize talk on CTIS provides an opportunity for sponsors to learn about user access and role management functionalities in CTIS. It covers:

  • how to manage the registration process;
  • how to navigate the different roles and permissions and their hierarchy within the system (as CTIS is as a role-based system).

Sponsors will have opportunity to ask questions during the event.

In order to make the best out of this session, attendees and viewers are highly recommended to make use of the following components in advance:

  • CTIS Sponsor handbook
  • Online training module 03 - User access management
  • Online training module 07 - Management of registered users and role matrix

The event is open to all sponsor organisations, including pharmaceutical companies, contract research organisations, small and medium-sized enterprises (SMEs) and academic organisations.

The Clinical Trials Information System (CTIS) will act as a single entry point for clinical trial authorisation and supervision in the European Economic Area. CTIS is the business tool of the EU Clinical Trials Regulation (Regulation (EU) No 536/2014).

EMA cannot provide attendees certificates of attendance for this event.

Event will be live broadcast, no registration is required for those wishing to follow the live broadcast on EMA’s website.

A video recording is made available after the event.

Attendees are invited to fill out a short feedback survey that will be available after the event on this page.

Video recording

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