MDD Devices

Device Vigilance System Update - Details from Acorn Regulatory

Device Vigilance System Additional Guidance: An Update from Our Devices Team

While much of the medical device industry is focused on MDR, the MDD is still in effect.  Our medical devices… Read more

LRQA medical device

Impacted By The LRQA Decision? Here Is How We Can Help

The decisions by Lloyd’s Register Quality Assurance (the LRQA) and QS Zurich that they will both will cease to offer… Read more

Acorn Regulatory has published its first medical device regulations (MDR) whitepaper.  The whitepaper looks at a range of issues. Get The Acorn Regulatory Medical Device Regulations Whitepaper

Get The Acorn Regulatory Medical Device Regulations Whitepaper

The new medical device regulations (MDR) will come into force in May 2020.  In advance of the deadline, companies across… Read more

Acorn Regulatory has published its first medical device regulations (MDR) whitepaper.  The whitepaper looks at a range of issues. Get The Acorn Regulatory Medical Device Regulations Whitepaper

Get The Acorn Regulatory Medical Device Regulations Whitepaper

The new medical device regulations (MDR) will come into force in May 2020.  In advance of the deadline, companies across… Read more

Understanding MDR: 8 Important Changes

The advent of the new Medical Devices Regulation (MDR 2017/745) is a cause of much concern for manufacturers and others… Read more

EU Authorized Representative – Find Out What You Need To Know As Brexit Nears

In recent months we have assisted a large number of companies in transferring their EU Authorized Representative from the UK… Read more

2018’s Most Read Medical Device Articles from Acorn Regulatory

The Acorn Regulatory medical devices team has grown again in 2018 and in the past 12 months we have worked… Read more

Authorised Representative EUDR New EU Medical Device Regulations_ The Impact for Economic Operators

Brexit & Notified Bodies – What Are The Implications for the Medical Devices Sector?

The implications of Brexit will, possibly, be felt most in the area of Notified Bodies.  The UK’s exit from the… Read more

What You Need To Know About the EU MDR & The Authorised Representative

Two new EU Regulations entered into force on 26th May 2017. Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU)… Read more

Contact us and enjoy a faster, smoother journey through the maze of European Pharmaceutical and Medical Device legislation with us as your expert guide.
©2021 Acorn Regulatory Consultancy Services Ltd. Company Registration No. 397294 VAT Registered No. IE 6417294V
Designed by