Great BritainNavigate Great Britain
Your trusted partner for UK market access
Successfully enter the UK market with confidence. Our UK-based regulatory experts provide comprehensive support for medical devices, IVDs, and cosmetics in the post-Brexit regulatory landscape.
Why Choose the UK Market?
Strategic advantages in post-Brexit Britain
Regulatory Agility
Faster regulatory decisions and innovative pathways with MHRA's streamlined processes and digital-first approach.
Global Gateway
English-speaking market with strong international connections and established trade relationships worldwide.
Innovation Focus
Government commitment to life sciences with significant R&D investment and supportive regulatory environment.
Speed to Market
Streamlined UK-specific pathways often provide faster market access compared to other major markets.
UK Post-Brexit Regulatory Framework
Navigate the evolving UK regulatory landscape with expert guidance. Our local presence ensures you stay compliant with all UK-specific requirements.
UK Medical Device & IVD Regulation
UK MDR 2002UK-specific medical device regulations following Brexit, maintaining high safety standards while enabling innovation.
Key Requirements
- UK Responsible Person (UK RP) required
- MHRA registration mandatory
- UK conformity marking (UKCA)
- Great Britain conformity assessment
UK Cosmetics Regulation
UK CR (EC) No 1223/2009UK cosmetics regulations ensuring product safety while supporting business growth and innovation.
Key Requirements
- UK Responsible Person required
- SCPN notification (Submit Cosmetic Product Notifications)
- Safety assessments
- OPSS compliance
Our UK Market Access Services
Comprehensive support for successful British market entry
UK Responsible Person
Complete UK RP services for all regulated products
Key Features
- MHRA liaison
- UK regulatory compliance
- UKCA marking support
MHRA Registration
Expert registration services with UK authorities
Key Features
- Database submissions
- Document verification
- Regulatory correspondence
Do you need a UK Responsible Person in addition to an EU Authorized Representative?
Our FAQ explains how the two roles differ.
Read the UK Responsible Person FAQ
Ready to Enter This Market?
Let's discuss your market entry strategy
Our regulatory experts are ready to help you navigate the path to market success.