I’ve been working on the HeSANDA project as part of the USYD-SHP team. Initial focus is to establish national infrastructure through a network of ‘nodes’ that curate and share IPD from clinical trials.
We are nearing the end of the Design phase with implementation slated to kick off in 2022.
– How many others are linked into this initiative?
– What formalised platforms and processes are in use across our groups for data sharing?