Clinical Trials Information System (CTIS) will act as the single entry point for clinical trials authorisation and supervision in the EEA.
How sponsor organisations can prepare for CTIS?
WHAT IS IT ABOUT?
Topics presented during the webinar include how sponsor organizations 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.
WHO CAN PARTICIPATE?
This EMA-hosted webinar is open to all sponsor organisations, including pharmaceutical companies, contract research organisations, small and medium-sized enterprises (SMEs) and academic organisations.
Check out the Agenda here
HOW TO REGISTER?
Registration is not needed, the event is broadcast live.
HOW & WHEN?
Date: 29/07/2021
Location: Virtual meeting, 14:00-16:30 (CEST)
CERTIFICTION?
No certificates of attendance will be issued for this event.
LIVE WEBCAST (PAGE) LINK
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