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Join ANDHealth and expert speakers from the TGA to hear an overview of the key changes in the updated SaMD regulations, and participate in a live Q&A session directly with the TGA.
This joint TGA-ANDHealth initiative will support Australian SMEs to navigate the regulatory guidelines and compliance requirements for Software as a Medical Device (SaMD).
This is an important session to attend for all Australian digital health SMEs required to design and deliver robust clinical trials and evidence to support the safety and efficacy of their digital health products, as verified by the TGA. Come along to have your questions answered and provide feedback to the TGA.
These sessions are running again this year, after high demand from those who missed out on last year’s booked out events. So register early; don’t miss out.
Resources:
For the current draft guidance, please visit: https://www.tga.gov.au/regulation-software-based-medical-devices
To test out the new "Is my Software regulated" flow chart, please visit: https://www.tga.gov.au/sites/default/files/my-software-regulated.pdf
Session format
Sign up for session time below:
