Safeguarding rights in genomics
Genomic information is deeply personal. It can reveal insights about an individual’s health, their family and future risks. Protecting people’s rights and information is essential for building trust and ensuring benefits are shared fairly. Informed consent and privacy form the foundation of responsible genomics in Australia.
Ethics
Using genetic information requires more than scientific accuracy – it demands ethical safeguards that protect people and respect cultural values. Ethical practice ensures that genomic data is used in ways that benefit individuals and communities rather than causing harm. Genomics Australia is committed to embedding cultural safety, promoting equity and making sure decisions are guided by clear standards that uphold the public’s confidence in how genomics is applied.