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MedTech
Value of MedTech
What is a medical device
Publications & Reports
Value of MedTech Report
Digital Health Report
Value-Based Procurement in Australia Report
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Why ESG Matters for Medtech in the Asia-Pacific Region
Prescribed List
Industry Development
Issues
Industry Policy
Industry Development
Regulatory
Current Issues
Regulatory Reforms
Advertising
UDI
Cyber Security
Clinical Trials
Standards
AS 5182: 2018 Vendor credentialing for healthcare facilities
AS/NZS 3551 and AS/NZS 2500 - ongoing issues
Medical Device Patient Information Materials
Private Health Insurance
Devices in Public Hospitals
Digital Health
Code of Practice
About the Code
Code Authority Guidance Docs
Explanatory notes and FAQs
Complaints
Archived publications
Training
Professional Development
Training Module Library
Instructions
Upcoming Courses
Events
Upcoming Events
Event Sponsorship
Australian Industry Awards
MTAA Annual Conference
Aus. Reg. Device Summit 2025
MedTech Story
Media
Latest
Media Releases
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WiMT
Women in MedTech
Mentoring Program
Gender Diversity
Women in MedTech Awards
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MTAA Annual Report 2016/17
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14/12/2017 11:24
Therapeutic Goods Amendment (2017 Measures No. 1) Bill 2017
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17/1/2018 08:21
Development of a Framework for Secondary Use of My Health Record Data
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Value-Based Healthcare Summit Sponsorship Prospectus
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TGA Consultation - Clinical evidence guidelines Medical devices - February 2016
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10/6/2016 11:13
TGA Consultation - Changes to accessing unapproved therapeutic goods through the Authorised Prescriber (AP) and Special Access Schemes (SAS)
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Therapeutic Goods Amendment (2016 Measures No.1) Bill 2016
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TGA Consultation – Enhancing sanctions and penalties in the TG Act 1989
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31/5/2017 10:43
TGA Consultation - Options for the future regulation of “low risk” products
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12/5/2017 11:45
TGA Consultation – Comparable overseas regulators – medical devices
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30/6/2017 11:53
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