Delivered in partnership with Mark Flynn (Global Edge Medtech Consulting), this intensive course is designed for innovators ready to take their medical device to market. Learn how to implement a QMS, navigate regulatory pathways in Australia, the EU, and USA/FDA, raise capital, and overcome manufacturing challenges. Build a comprehensive portfolio including a go-to-market strategy, pitch deck, regulatory pathway, and clinical strategy. Ideal for CEOs, founders, CTOs, and leaders in medtech with TRL 4–7 projects.
🗓️ Date: (3 – 5 March 2026)
✍️ Deadline for application: Feb 13 2026.
By the end of this course, you will understand how to:
- Implement a QMS into your medical device process
- Identify your pathway to market in Australia, EU and/or USA/FDA
- Raise capital and apply for grant funding
- Navigate the specific challenges of manufacturing a medical device
- Build relationships with partners, consumer advocates, advisory boards
- Build a portfolio of work including a go-to-market strategy, pitch deck, regulatory pathway and clinical strategy
