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Ensuring Compliance and Confidence: MedTech & QMS Certification
In the highly regulated world of medical technology, maintaining uncompromising quality standards is not just good practice, it’s a legal necessity. A Medical Device Quality
Navigating MedTech Product Recalls – Managing the Risk with Confidence
Earlier this year Australia’s medical device landscape entered a new era of post-market regulation. On 5 March 2025, the Therapeutic Goods Administration (TGA) implemented the
Protecting the Pulse of Innovation: Why Strong IP Strategies Are Vital for MedTech Success
The medical technology (medtech) industry is transforming health care at an unprecedented pace. Artificial intelligence, data analytics and 3D printing are no longer futuristic concepts
TGA Essential Principles Checklist: What do you need to know
The Therapeutic Goods Administration (TGA) has introduced a major update to the Essential Principles (EP) checklist for medical devices and in vitro diagnostics (IVDs), effective
Medicinal Cannabis Regulation for Clinicians – Your Guide as a Prescriber
As medicinal cannabis becomes a more common treatment option in Australia, healthcare practitioners face increasing scrutiny from regulators and medical boards. Understanding the rules around
Medicinal Cannabis Businesses in Australia – What you need to know
Helping Cannabis Businesses Succeed Within Australia’s Regulatory Framework The Australian medicinal cannabis industry presents significant commercial opportunity, but also complex regulatory risk. From licensing, warehousing