Medical Device Regulations for Non-Regulatory Professionals Workshop | 1 May 2026
Navigating medical device regulation doesn’t have to be daunting, even if it’s not your day job. This highly interactive workshop is designed specifically for non-regulatory professionals to build a practical, real-world understanding of how regulation shapes product development, marketing, and post-market activity. Through engaging case studies and hands-on activities, participants will demystify the medical device regulatory landscape. Most importantly, the session equips attendees with the confidence, language, and tools to work more effectively with regulatory teams, asking better questions, spotting issues earlier, and strengthening cross-functional collaboration to improve outcomes for both your organisation and patients you serve.
Who Should Attend?
- Entry-level regulatory professionals
- MedTech professionals outside of regulatory departments:
- Business Development Managers
- Marketing Specialists
- Quality Professionals
- Clinical Specialists
- R&D (Research and Development) Teams
- Supply Chain and Logistics Professionals
- Legal and Compliance Officers
Note: This is a face-to-face event with no recordings available. Placements are strictly limited.
Workshop Schedule
To maximise access, this workshop will be offered in two identical sessions:
- Morning: 9:00am–1:00pm
- Afternoon: 12:00pm–4:00pm
Attendees from both sessions will come together for a shared networking lunch from 12:00pm–1:00pm, creating a valuable opportunity to connect across cohorts.
Both sessions cover the same content.
Registration
- Members $295 incl. GST per person
- Non-Members $350 incl. GST per person
