Clinical Trials Information System (CTIS) bitesize talk: Document and personal data in CTIS
EventHumanClinical trials
- The original event time is:
- Thursday, February 23, 2023 - 14:30 - 16:00 Amsterdam time (CET)
Date
- , -
Location
- OnlineEuropean Medicines Agency, Amsterdam, the Netherlands
Event summary
CTIS is the business tool of the EU Clinical Trials Regulation (Regulation (EU) No 536/2014) and it acts as a single entry point for clinical trial authorisation and supervision in the European Economic Area.
This bitesize talk on CTIS provides an opportunity for sponsors to learn how to use the ‘Publication’ and ‘Not for publication’ requests and remove personal data from Document properties. Sponsors will also be able ask questions on this CTIS topic during the event (Slido code will be provided during the event).
To be better prepared for this event, sponsors are encouraged to consult the CTIS training and support materials.
The event is open to all sponsor organisations, including pharmaceutical companies, contract research organisations, small and medium-sized enterprises (SMEs) and academic organisations. EMA cannot provide participants certificates of attendance for this event.
CTIS Bitesize talks are live broadcast and no registration is required for those wishing to follow the live broadcast on EMA’s website.