Core outcome sets (COS)
A COS is a minimum set of outcomes of specific importance that should be measured and reported in all clinical trials for a specific condition. COS are developed with the input of relevant stakeholders, and patient engagement is a central part in the process of COS development. Read more
Prioritization of evidence gaps using the James Lind Alliance method
SBU’s work in bringing patients, consumers, carers and profession together in identifying and prioritising the most important evidence gaps in their area. Read more