Rare Disease Day

Rare Disease Day

More than 300 million people worldwide and two million Australians live with rare disease, and 72% of rare diseases are genetic. This internationally recognised day of awareness has been building support for the rare disease community since 2008 and calls for...
Looking forward to 2023

Looking forward to 2023

As we start the new year, InGeNA continues our mission to realise the full potential of genomics to personalise healthcare. This year we look forward to working closely with our partners to advocate for the benefits genomics can bring to both patient outcomes and...
Welcome to our new Chair

Welcome to our new Chair

InGeNA welcomes one of Australia’s leading digital health executives Kathy Campbell (Director, Ockham Consulting) to take on the role of Chair for 2023-24.Our inaugural independent Chair David Bunker is stepping down after more than two years in this important...
December Quarterly Forum

December Quarterly Forum

Our final quarterly members forum for 2022 is scheduled for Thursday 15 December, 4:00pm – 5:00pm AEDT. At this forum we will hear from two collaborators who have recently been awarded MRFF grants. InGeNA provided a letter of support to each of these...