Supporting your introduction of compliant medical devices
The medical device industry is entering its most significant period of regulatory change since the 1990s. While the new regulatory landscape will bring complex challenges for manufacturers, it will also introduce essential changes designed to enhance patient safety and enable the introduction of more innovative medical device solutions.
We recognise that every organisation is unique, and we understand that the impact of the new medical device regulations will depend on the complexity of your organisation. We take the time to understand your organisation, using analytical precision to achieve the best outcomes for you and your clients.
LR's experts regularly share their research and insights.
Who we work with
We help thousands of organisations, from the world's best known brands to the smallest of suppliers. How can we help you?
Putting the patient first at Penlon.
Putting the patient first. Auditor training to transition to the latest ISO quality management system standard for medical devices. See how in our case study.
Our latest updates
Shares in Advanced Oncotherapy PLC rise following ISO 13485 certification
Advanced Oncotherapy PLC shares rise following ISO 13485 certification
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22 May 19
Confined Spaces: An Expert Forum
4 Jun 19
10 Sep 19