Medical Device Regulations for Non-Regulatory Professionals Workshop | 4 June 2026
Navigating medical device regulation doesn’t have to be daunting, even if it’s not your day job.
Join us for this practical, streamlined session designed to give non-reg professionals a clear, practical understanding of the regulatory landscape across pre-market, post-market, advertising and communications.
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.
You’ll also hear from industry expert Jasjit Baveja, Director of Regulatory and Industry Policy bringing real-world insight to help translate regulation into business impact, and guest speaker Kea Dent, Director at KD&A.
Agenda
- 9:00am -- Workshop Start
- 9:00am-9:30am -- Introduction
- 9:30am-10:30am -- Pre-Market
- 10:30am-11:00am -- Morning Tea
- 11:00am-11:45am -- Post-Market Session
- 11:45am-12:30pm -- Advertising
- 12:30pm-1:00pm -- Communication
- 1:00pm-2:00pm -- Networking Lunch
- 2:00pm Finish
Who Should Attend?
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.
Registration
- Members $295 incl. GST per person
- Non-Members $350 incl. GST per person
Contact Information
Additional Information
Your Speakers
Jasjit Baveja is Director of Regulatory and Industry Policy at MTAA, where she leads regulatory policy development and industry engagement with the Therapeutic Goods Administration. She brings over a decade of hands-on experience in medical device regulation.
A long-standing advocate for women in the medical technology industry, Jasjit has co-led women’s network employee resource groups at both Boston Scientific and Johnson & Johnson, and continues to champion gender diversity and inclusion across the sector through her work at MTAA.
In 2003 Kea established KD&A an Australian based consulting firm offering medical device regulatory solutions for manufacturers, sponsors, legal representatives, and distributors around the world. As a regulatory and Quality Management System (QMS) specialist for medical devices and IVDs, Kea's expertise lies in obtaining TGA and global regulatory product certifications, ISO 13485/MDSAP QMS creation, implementation, certification, maintenance, and regulator audits. With over three decades of experience in the medical device sector, Kea possess a wealth of expertise, having worked as both a medical device manufacturer and regulatory consultant.
Kea's journey commenced in 1993 when she setup and managed a medical device manufacturing business. Over the subsequent decade she navigated the medical device regulatory landscape firsthand as a device manufacturer, acquiring and upholding numerous product certifications (CE Marking as per the Medical Device Directive 93/42/EEC (obtained in 1998), 510(k), TGA and Health Canada certifications, etc.) and QMS/MDSAP certifications crucial for market access to over 44 countries. In 2003 the 95% export medical device manufacturing business was sold to a Canadian competitor.
Kea's personal success is displayed through her 2002 selection as the winner of the South Australian Telstra Business Woman of the Year Award in the private sector category.
