The Core Curriculum: Essential MDR Compliance Training for Medical Device Distributors
Navigating the complexities of the European Union Medical Device Regulation (MDR) requires a well-informed and competent team, especially for medical […]
EU MDR – Essential Staff Training and Compliance for Medical Device Distributors
The European Union Medical Device Regulation (MDR) 2017/745 introduces significant changes and stricter requirements for all economic operators in the […]
Post-Brexit Medical Device Regulations: What’s Changed?
The United Kingdom’s departure from the European Union (Brexit) has fundamentally altered the regulatory environment for medical devices. For all […]
Impact of Brexit MDR UK Distributors
The departure of the United Kingdom from the European Union (Brexit) has created a new regulatory landscape for medical devices, […]
MDR vs MDD: Key Changes Distributors Need to Understand
The European Union Medical Device Regulation (MDR) (EU) 2017/745, which took effect on May 26, 2021, represents a significant overhaul […]
Ensuring Accountability: MDR Traceability Requirements and Record-Keeping for Distributors
Introduction Within the evolving framework of medical device regulations, the European Union Medical Device Regulation (MDR) 2017/745 places a significant […]