Medical Device Regulatory Workshops Melbourne | 1 - 5 December 2025

9:00am Monday, 1 December 2025
5:00pm Friday, 5 December 2025
MedTech Workshop
Cliftons Melbourne - Collins Street
1/440 Collins St
Melbourne, Victoria 3000
Australia

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.

 
Pre-Market (Monday, 1 December 2025)

Monday, 1 December 2025, 9:00am - 5:00pm

Learning outcomes 

  1. Basics of Australian Medical Device Regulations and TGA structure and personnel 
  2. Leveraging comparable overseas regulator approvals for TGA applications 
  3. TGA applications, variation applications, and application audits – best practice guidelines for a good submission 
  4. TGA CA applications - best practice guidelines for a good submission 
  5. Case studies 
  6. Q&A with TGA 
 
Post-Market (Tuesday, 2 December 2025)

Tuesday, 2 December 2025, 9:00am - 5:00pm

Learning outcomes

  1. Adverse events - definitions, sponsor and manufacturer responsibilities, TGA report review process  
  2. Recalls - flow, types, decision-making about outcomes   
  3. Reviews, safety, reclassification, managing feedback on reforms 
  4. Q&A with TGA 
 
SaMD (Wednesday, 3 December 2025)

Wednesday, 3 December 2025, 9:00am - 5:00pm

Learning outcomes

  1. Overview of SaMD regulation 
  2. Classification rules 
  3. Software carve-out 
  4. Clinical Decision Support System (CDSS) 
  5. Evidence, artifacts, AI, cybersecurity 
  6. Q&A with TGA 
 
Clinical Evidence (Thursday, 4 December 2025)

Thursday, 4 December 2025, 9:00am - 5:00pm

Learning outcomes

  1. Pre-clinical requirements 
  2. Post-clinical requirements 
  3. Q&A with TGA 
 
Medical Device Regulatory Basics for Startups (Friday, 5 December 2025)

Friday, 5 December 2025, 9:00am - 5:00pm

More details will be available soon.

 

Who Should Attend?

  • MedTech Regulatory Professionals
  • Academia / Students focused on the medical device industry
  • Small business owners with regulatory responsibilities
  • Startups/entrepreneurs

Note: These are face-to-face workshops, there are no recordings available. Placements are strictly limited.


Registration

The series offers a choice of 5 workshops, priced for members and non-members. Discounts are available for those attending the entire week.

4-Day Workshop Registration (Monday, 1 December - 4 December 2025)

  • Members $3,564 incl. GST per person (includes all workshops excl. Startup Workshop)
  • Non-Members $4,633 incl. GST per person (includes all workshops excl. Startup Workshop)

Day Registrations

  • Members $990 incl. GST per person per workshop
  • Non-Members $1,287 incl. GST per person per workshop

Startup Workshop Only (Friday, 5 December 2025)

  • Members $750 incl. GST per person
  • Non-Members $975 incl. GST per person

Terms and Conditions

Contact Information