This is a practical workshop designed for those in sales, marketing, product development, and other non-regulatory roles who need to understand Australia's medical device regulations. Through interactive case studies, real-world scenarios, and hands-on activities, participants will learn how medical devices are classified, the pathways used to bring them to market, and key compliance requirements. The workshop will also focus on effective collaboration with regulatory teams to ensure business success while meeting TGA regulations.

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.

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.