Regulatory affairs and health economics workshop
Monday 30 April 2018 - Adelaide Convention Centre
AusMedtech, the national industry group representing the medical devices and diagnostics industry sector in Australia, invites you to attend the Regulatory Affairs and Health Economics Workshop at AusMedtech 2018.
While Australia boasts a strong market for developing medical technology, yet the landscape is complex and dynamic. This workshop will explore this landscape, presenting current trends and emerging issues that may affect organisations operating in the medical device industry.
Brandwood Biomedical will lead the morning session, focusing on the Therapeutic Goods Administration (TGA)’s Medicines and Medical Devices Review (MMDR), changes in the European Union (EU) and provide an overview of risk classification.
The afternoon session, led by Sarah Griffin, Principal consultant, reimbursement, Brandwood Biomedical , will discuss prostheses prices and continuing reform of private health insurance.
If you are attending the conference as well as the workshop, please register via the conference registration page (AusMedtech 18 delegates receive a discounted registration for the workshop)
If you wish to attend the workshop only, please register via the link below
Regulatory affairs (morning session, 3.5 hours)
- TGA medical device reform
- Changes in the EU
- How are devices regulated?
- Risk classification overview
- How to get approved in Australia
- Leverage TGA approval internationally
Health economics (afternoon session, 3.5 Hours)
- How can I get paid?
- Reimbursement framework: public, private and other
- Applying for reimbursement: what you need to do
- Clinical evidence requirements
- What’s changing?
Member attending the conference: $300 AUD incl. GST
Non-member attending the conference: $380 AUD incl. GST
Member workshop only: $500 AUD incl. GST
Non-member workshop only: $580 AUD incl. GST