by elena@investinu.ie | Sep 6, 2021 | Acorn Regulatory News, Medical Devices
The Unique Device Identifiers system under the Regulation (EU) 2017/745 (MDR) and Regulation (EU) 2017/746 IVDR applies new requirements on all participants of the supply chain. The overall objective of which is to improve patient safety by means of better...
by elena@investinu.ie | Dec 6, 2020 | Acorn Regulatory News, Brexit, Medical Devices
How will the Northern Ireland Protocol impact companies in the medical devices sector? That is a question that we have been asked many times in recent months. Now, as the UK’s departure from the EU gets closer, we have created a brief guide on the Northern Ireland...
by elena@investinu.ie | Dec 1, 2020 | Acorn Regulatory News, Brexit, Medical Devices
Our clients have been contacting us in recent weeks with questions relating to the Northern Ireland Protocol and medical devices. They are eager to understand the intricacies of the Northern Ireland Protocol and how it will impact their companies. We have gathered...
by elena@investinu.ie | Aug 6, 2020 | Acorn Regulatory News, Medical Devices
The Unique Device Identifier system under Regulation (EU) 2017/745 (MDR) and Regulation (EU) 2017/746 IVDR applies new requirements on all participants of the supply chain with the final aim of improving patient safety through better traceability and transparency....
by elena@investinu.ie | Aug 6, 2020 | Acorn Regulatory News, Medical Devices
The Unique Device Identifier system under Regulation (EU) 2017/745 (MDR) and Regulation (EU) 2017/746 IVDR applies new requirements on all participants of the supply chain with the final aim of improving patient safety through better traceability and transparency....
