Don’t Miss Out: MTAA’s 2025 Medical Device Regulatory Workshops Are Here!

The regulatory landscape is changing fast—is your business keeping up?
The MTAA Medical Device Regulatory Workshops 2025 are a series of TGA-led sessions designed to provide comprehensive insights into the evolving regulatory landscape for medical devices in Australia. These workshops aim to equip MedTech Professionals and MedTech Startups with the latest updates, compliance strategies, and best practices to navigate regulatory requirements effectively. Attendees will gain valuable knowledge on pre-market, post-market, software as a medical device, clinical evidence and medical device regulatory basics for startups.
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The series offers a choice of 5 workshops, priced for both members and non-members. Discounts are available for those attending the entire week. Startups also receive a discount for attending the Medical Device Regulatory Basics for Startups workshop. Special Introductory Rates available for students.
What topics will be covered in the 5 days?
- Day 1: Pre-Market
- Day 2: Post-Market
- Day 3: SaMD
- Day 4: Clinical Evidence
- Day 5: Medical Device Regulatory Basics for Startups
Who Should Attend?
- MedTech Regulatory Professionals
- Academia / Students focused on the medical device industry
- Small business owners with regulatory responsibilities
- Startups/entrepreneurs
Note: These are face-to-face workshops; there are no recordings available. Placements are strictly limited.
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