• Flow chart - Overview of the medical device regulatory process
  <http://www.tga.gov.au/devices/process.htm>
• How do I determine whether my product is a 'therapeutic good'?
  <http://www.tga.gov.au/docs/html/determine.htm>
• An overview of the new medical devices regulatory system
  <http://www.tga.gov.au/docs/html/devguid1.htm>
• Obligations and responsibilities of medical device sponsors and manufacturers
  <http://www.tga.gov.au/docs/html/devguid20.htm>
• Transitional arrangements for the introduction of the new medical devices regulatory system
  <http://www.tga.gov.au/docs/html/devguid9.htm>

Differences between the Australian and European Union regulatory systems

• Differences between the Australian and European Union regulatory systems (1) - Fundamental differences and classification
  <http://www.tga.gov.au/devices/fs-aeu-class.htm>
• Differences between the Australian and European Union regulatory systems (2) - Essential principles
  <http://www.tga.gov.au/devices/fs-aeu-ep.htm>