Abstract
The generation of robust evidence informing cancer prevention and treatment is premised on availability of patient-level data. Canadian policies and infrastructure limit cross-jurisdictional data sharing. Alongside efforts to enable greater access and use of patient data, understanding preferences for participation in such initiatives is critical. This qualitative investigation sought to elicit patient values, expectations, and concerns for enhancing pan-Canadian data sharing for precision oncology research.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
