IFAPP – WEBINAR: EU – CTR UPDATE WORKSHOP
Only 6 months left for transition!
![](https://amife.net/wp-content/uploads/2023/09/logo_IFAPP_crop.png)
Date: 27 June 2024
Time: 12:00 – 02:00 PM CEST
The “Clinical Trials Regulation”, Regulation EU 536/2014, has been valid since 31 January 2022 and mandatory since 31 January 2023. The “Transition Period” will end on 30 January 2025.
Practical experience of competent authorities and sponsors have detected deficiencies and gaps when applying for authorisation, authorising, supervising and reporting clinical trials in CTIS, the overarching Clinical Trials Information.
Moderator
DR. INGRID KLINGMANN. Introduction to new developments in the CTR framwork
Speakers
OSKIA BUENO ZARAGUETA. What has changed in CTIS (since March 2023) from EMA’s perspective?
NICOLE WOIK. Experience with working in CTIS, relevant changes and requirements for the sponsor
Register in advance for this webinar:
https://us02web.zoom.us/webinar/register/WN_U9r-DCsfQIu5EhfxfhViEA
After registering, you will receive a confirmation email containing information about joining the webinar.
TIME SCHEDULE
0 6 : 0 0 – 0 8 : 0 0 AM E S T
1 0 : 0 0 – 1 2 : 0 0 AM GMT
1 2 : 0 0 – 0 2 : 0 0 PM C E S T
0 7 : 0 0 – 0 9 : 0 0 PM J S T