How can sponsors ensure the consistency and traceability of all the information submitted to these various repositories? How do they organise their processes to deliver the required information in time with limited resources?
Many also question the purpose of these multiple registries and even argue that the original purpose of facilitating patients' access to clinical trials has not been met. Others suggest that industry and investors use the databases as competitive intelligence tools.
To provide perspective to these difficult questions, we are proud to present you a distinguished panel of speakers from academia, patients’ organisations and the pharmaceutical industry from several European and worldwide institutions.
Join us to discuss the status of clinical trial registries worldwide and to hear from the authorities that operate them. Listen to the real-life implementations in industry and academic institutions. Listen to the voice of the patients and learn about their expectations. Get insights into the development of worldwide information management standards for registries and discuss with us how worldwide registries can be harmonised and improved.
Event Code:
11114