Medical Device Regulatory Affairs Consulting and Services
About LRS
A boutique consultancy and regulatory affairs service provider for medical device manufacturers.
Our goal is to support your organisation’s needs by providing additional expertise for a specific project or stepping in to fill an interim role.
LRS strive to gain a deep understanding of your technology and product, integrating with your existing teams or operating independently to achieve compliance.
Centred on results, our regulatory advice is grounded in real-world experience across multiple device areas and proven success.
Link Regulatory Services Ltd specialise in (EU) MDR 2017/745 and UK MDR 2002 regulations.
“work was always diligently thought through with excellent attention to detail, prioritisation and knowledge”
Director, Class IIa medical device manufacturer SERVICES & EXPERIENCE
(EU) MDR 2017/745
UK MDR 2002
QUALITY MANAGEMENT SERVICES
OUR EXPERIENCE
CONTACT US
Get in touch so we can hear more about your medical device regulatory challenges and see how Link Regulatory Services Ltd can help.
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