LRQA

Your Route to Conformity
With more than 10 years' experience as a Notified Body for the Medical Device Directive and the In-vitro Diagnostic Directive, LRQA has established an in-depth level of knowledge and understanding.

With our involvement in national and European working groups, it gives us access to a wealth of information, enabling our dedicated product conformity team to keep you up to date with current and future market developments. With our experience we can help you plan for the future and ensure you meet regulatory requirements. So, if you're looking to comply with one of the Directives using a quality management system approach, we can help. Our assessors provide consistent and constructive audits to help ensure your system delivers tangible business benefits, while giving you the confidence that your system meets regulatory requirements.

Choosing LRQA means you'll be working with one of the world's most trusted and respected management system bodies providing you, your customers and other stakeholders with business assurance.

For more information visit us on stand 24 or view our website www.lrqa.co.uk for testimonials and case studies.