About UKRP Service – Your Trusted UK Responsible Person (UKRP) Provider

Welcome to UKRP Service, a leading provider of UK Responsible Person (UKRP) services for medical devices and cosmetics entering the UK market. We specialize in ensuring full compliance with the UK Medical Devices Regulations (UK MDR 2002) and UK Cosmetics Regulation, helping global manufacturers navigate post-Brexit requirements efficiently.

The Expertise

At Eomi Consultancy, we specialise in regulatory and quality management services for Medical Devices, Cosmetics, and Food Supplements. With extensive experience and a proven track record of successful MHRA inspections, we provide end-to-end support to help your products comply with UK regulations. Our services include:

  • UK Responsible Person (UKRP) Services – Acting as your UKRP for Medical Devices, ensuring compliance with the latest UK regulations following Brexit, and handling MHRA registrations for medical devices.
  • MHRA Registration Support – Assisting in the registration process for Medical Devices with the MHRA to ensure compliance with UKCA marking requirements and regulatory submissions.
  • UK Cosmetics Notifications – Supporting your UK cosmetics products with the notification process to the MHRA, ensuring compliance with UK cosmetic regulations.
  • Global Market Entry for Food Supplements – Successfully launching products in the UK, EU, US, and Asia.
  • Quality Management Systems – Implementing robust QMS tailored for Medical Devices, Cosmetics, and Food Supplements.
  • Regulatory Artwork & Formulation Reviews – Conducting in-depth reviews across multiple product classifications, including cosmetics and medical devices.
  • UKCA & MDR Compliance – Developing technical files for UKCA and MDR regulatory submissions, including UKRP services for medical devices.
  • Regulatory Audits & Technical File Reviews – Assisting with evaluations by MHRA, Notified Bodies, and competent authorities to ensure your products meet regulatory standards.
  • ISO Certifications – Helping you achieve ISO 13485, ISO 9001, ISO 14001, and ISO 27000 certifications.
  • Product Registrations – Facilitating product registrations with UK and EU competent authorities, including acting as your UKRP for medical devices.

What we do

We specialise in providing ongoing support to FMCG companies, with a primary focus on medical devices and cosmetics. Our expertise extends across marketing, supply, logistics, and sales teams, ensuring seamless end-to-end compliance with UK Medical Device Regulations (UK MDR 2002, SI 2002/618), EU Medical Device Regulation (EU MDR 2017/745), UK Cosmetics Regulations (Cosmetics Regulation (EC) No. 1223/2009 as retained in UK law), EU Cosmetics Regulation (EC) No. 1223/2009, and UK Food Supplement Regulations (The Food Supplements (England) Regulations 2003), while enhancing regulatory knowledge throughout your business.

Book a UKRP Compliance Review

UK Responsible Person

EU Authorised Representative

UK MDR Compliance

Regulatory Strategy

Formulation Review

Technical File Review

Claims Review

Product Registration

Labelling Review

INNOVATIVE

At UKRP Service, we provide customised solutions that empower you to launch your product in your target market. Our forward-thinking approach ensures all projects are designed with the future in mind, supporting your company's growth and expansion every step of the way.

ORGANISED

We take pride in our organisation and transparent communication with clients. We ensure clear project timelines, defined deliverables, and continuous visibility into progress, keeping you informed every step of the way.

KNOWLEDGEABLE

Our experienced team provides expert guidance to ensure your regulatory requirements are met. We stay informed about the latest regulations and offer valuable insights into upcoming changes or amendments to keep your business ahead of the curve.

INCLUSIVE

We collaborate closely with your company to ensure our solutions are seamlessly integrated across all functions. While regulatory projects often operate in silos, we focus on a smooth implementation that benefits every department and drives overall success.