The Australian Therapeutic Goods Administration (TGA) is implementing Unique Device Identification (UDI) requirements for medical devices sup...
Navigating the New MDSAP Audit Approach (v.10)
The landscape of global medical device compliance officially shifted on February 2, 2026. With the U.S. FDA’s Quality Management System Regul...
UK MHRA Proposes Indefinite Recognition for CE-Marked Devices
The UK’s regulatory landscape for medical devices just took a major leap toward long-term certainty. On 16 February 2026, the MHRA released a...
