E
EMA Events
Guest
This bitesize talk on CTIS provides an opportunity for sponsors to learn about modifications to clinical trial applications in CTIS.
Sponsors will have opportunity to ask questions during the event.
The event is open to all sponsor organisations, including pharmaceutical companies, contract research organisations, small and medium-sized enterprises (SMEs) and academic organisations.
Sponsors are encouraged to consult the CTIS training and support materials, including the CTIS sponsor handbook and online modular training programme prior to attending this event.
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.
A video recording is made available after the event.
Sumber : https://www.ema.europa.eu
Sponsors will have opportunity to ask questions during the event.
The event is open to all sponsor organisations, including pharmaceutical companies, contract research organisations, small and medium-sized enterprises (SMEs) and academic organisations.
Sponsors are encouraged to consult the CTIS training and support materials, including the CTIS sponsor handbook and online modular training programme prior to attending this event.
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.
A video recording is made available after the event.
Sumber : https://www.ema.europa.eu