Medical Device Regulatory Affairs Services
About LRS
A regulatory affairs service provider and boutique consultancy 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
UK MDR 2002
(EU) MDR 2017/745
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.
CONTACT OPTIONS
Book a free 30 min consultation
Request a call back to hear from a Regulatory Affairs Expert
Make an enquiry directly to a member of the team below