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!

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Essential Regulatory Workshops in Sydney and Melbourne 

Join us for the Essential Medical Device Regulatory Workshops in Sydney and Melbourne, where industry professionals will gain critical insights into the ever-evolving regulatory landscape. From 10-14 November in Sydney and 1-5 December in Melbourne, these five-day events will feature expert-led sessions on the latest regulatory updates, compliance strategies, and best practices for successfully bringing medical devices to market. Don’t miss this opportunity to enhance your knowledge and stay ahead of industry trends. Spaces are limited, so secure your spot today! Click to learn more and register for these pivotal workshops.

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