Medical Device Regulatory Workshops Melbourne | 28 April - 2 May 2025

9:00am Monday, 28 April 2025
5:00pm Friday, 2 May 2025
MedTech Workshop
TBC
TBC
TBC, Victoria TBC
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, 28 April 2025)

Monday, 31 March 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, 29 April 2025)

Tuesday, 1 April 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, 30 April 2025)

Wednesday, 2 April 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, 1 May 2025)

Thursday, 3 April 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, 2 May 2025)

Friday, 4 April 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 contains a choice of 5 workshops, priced for members and non-members. There are discounts available for those attending the entire week.

4-Day Workshop Registration (Monday, 28 April - Thursday, 1 May 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 $999 incl. GST per person per workshop
  • Non-Members $1,287 incl. GST per person per workshop

Startup Workshop Only (Friday, 2 May 2025)

  • Members $890 incl. GST per person
  • Non-Members $1,158 incl. GST per person

Terms and Conditions

Contact Information

Additional Information

 
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