Have your say: MTAA Medical Device Regulations for Non-Regulatory Professionals Workshop

We understand the struggle—explaining medical device regulations to sales, marketing, and product teams can feel like an uphill battle. They need to understand the rules, but deep dives into TGA classifications and compliance pathways make their eyes glaze over.

Here’s the solution: MTAA’s “Medical Device Regulations for Non-Regulatory Professionals” Workshop on the 21st of May 2025. This interactive, hands-on session is designed to help your colleagues grasp what actually matters—how devices are classified, the pathways to market, and how to work with you to stay compliant without roadblocks.

💡 Help us tailor this workshop to address your biggest pain points! Take this quick survey to tell us what you wish your non-regulatory colleagues knew:

🔗 https://forms.office.com/r/sGsLvMDiLM

Let’s make working with non-regulatory teams easier, not harder!