Updated Records of Clinical Trials Information System (CTIS) Webinar about How Sponsor Organisations can Prepare for CTIS

On 13 August 2021 the EMA updated the records of the CTIS webinar event.

Clinical Trials Information System (CTIS) will act as the single entry point for clinical trials authorisation and supervision in the EEA. CTIS was created as part of the EU Clinical Trials Regulation (Regulation (EU) No 536/2014).

Topics presented during the webinar include how sponsor organisations can prepare for CTIS, how Member States aim to support sponsor preparedness and adoption of CTIS, the role of the Clinical Trial Regulation and how sponsors can best make use of EMA’s CTIS training materials.

A recording of this event is available.

Read more online 
Copyright Widler & Schiemann AG 2020. All Rights Reserved. /