NPZ Technology Limited
NPZ Technology Ltd is a Cambridge-based medical device regulatory consultancy, MHRA-registered (No. 8269), specialising in cross-border regulatory support for medical device manufacturers seeking to access international markets — with a primary focus on the Great Britain market.
What We Offer
NPZ Technology provides regulatory consultancy services for medical device manufacturers navigating international market access requirements. Our primary expertise is in the Great Britain regulatory framework, with broader cross-border regulatory support available for manufacturers entering multiple markets.
Services include:
- UK Responsible Person (UKRP) appointments
- MHRA device registration (all device classes)
- PPON registration
- Certificate of Free Sale (CFS) procurement
- Regulatory compliance consulting and documentation
Products and services
UK Medical Device Regulatory Consultancy — UKRP, MHRA Registration & Market Access Services
NPZ Technology Ltd is a Cambridge-based medical device regulatory consultancy (MHRA registration No. 8269), providing cross-border regulatory support for medical device manufacturers seeking to access the Great Britain and international markets.
Our Services
- UK Responsible Person (UKRP) — Mandatory appointed representative for overseas manufacturers placing devices on the GB market under UK MDR 2002
- MHRA Device Registration — End-to-end registration support for all device classes (Class I, IIa, IIb, III, IVD)
- PPON Registration — Private Provider of Notified services registration and management
- Certificate of Free Sale (CFS) — Procurement and authentication of CFS documents for export purposes
- Regulatory Compliance Consulting — Technical documentation review, labelling requirements, post-market surveillance, and ongoing compliance support
NPZ Technology works with overseas medical device manufacturers to navigate the GB regulatory landscape efficiently, reducing time-to-market and ensuring full compliance with MHRA requirements.
