Medical Devices

The medical regulatory landscape is undergoing its most significant overhaul in years, and with that comes a need to stay up-to-date with the latest regulatory intelligence and how the changes impact your organisation.

As a leading Notified Body with over 20 years' experience in the medical arena, LRQA’s medical technical experts and industry specialists provide best-in-class medical quality assurance, CE Marking product certification to Medical Device Directive (MDD) 93/42/EEC and In Vitro Diagnostic Device Directive (IVDD) 98/79/EC, and training services that will equip you with the relevant knowledge at any stage of the product lifecycle, towards a timely market launch.

Unlike other Notified Bodies, our unique assessment approach ensures that we truly understand your long-term business objectives in order to reduce business risk, and enhance effectiveness, efficiency, and continuous improvement of your management systems.

As part of the Lloyd’s Register (LR) Group, LRQA’s work with medical directives, CE Marking, and quality assurance helps to ensure the safety of a range of consumer products and medical equipment, enabling us to contribute directly to a key part LR’s mission of protecting life and property.

To find out more about how LRQA can help you with your requirements, email us at