Symposium on Regulatory Fundamentals in Medical Devices

Tuesday, 28th August 2018, 9:00 am – 4:00 pm

This symposium, hosted by CSIRO, is designed to provide an introduction to regulatory fundamentals in the context of biomedical devices. The symposium will feature five speakers from the Therapeutic Goods Administration in Canberra that will focus on:

  • An introduction to medical device regulation
  • Process of conformity assessments for higher risk devices
  • Meeting clinical evidence requirements through translational research
  • Keeping Australia safe: continuing responsibilities
  • Applications of testing and standards to medical devices

Participants will also have the opportunity to join a tour of the new CSIRO Biomedical Manufacturing Translational Facility (BMTF) and other relevant CSIRO infrastructure.

This symposium provides a unique opportunity for everybody that is interested in translational aspects of biomedical devices to get an overview of the most important aspects of regulatory issues from TGA experts, all compressed into one day.

More information and registration


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