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MPS Medical-Product-Service UK Ltd

Full company profile

uuid004xecl

Namestring
MPS Medical-Product-Service UK Ltd
Legal namestring
MPS Medical-Product-Service (UK) Ltd
Websiteurl
mps-uk.uk
Company typeenum
Private
Founded yearstring
-
Descriptiontext

MPS Medical-Product-Service UK Ltd is a regulatory consulting firm headquartered in Devizes, Wiltshire, United Kingdom, founded in 2021. The company provides three core services to international medical device manufacturers: (1) UK Medical Device Responsible Person services, registering and maintaining devices with the MHRA; (2) EU MDR EC-REP services delivered through an affiliated German entity, MPS GMBH; and (3) US local representative services. The firm also develops tailored regulatory strategies and Quality Management Systems, and prepares Technical Files and Clinical Evaluation Filings for clearance across UK, EU, and USA markets. Its primary customer segment is international medical device companies, with secondary engagement from university spin-outs and start-ups requiring early-stage regulatory guidance.

The business operates as a low-overhead, relationship-driven professional services firm with a team of six, including three regional engagement leads (Ben Wensley-Stock for the UK, Gerhard Frömel for the EU, Reuben Lawson for the USA) each bringing 25-30 years of medical device industry experience. The go-to-market is direct and consulting-led, with the company's website as the primary marketing channel and direct contact (email and telephone) as the bottom-of-funnel conversion method. There is no proprietary software platform; the offering is entirely human-expertise-based. Pricing is quote-based and not publicly disclosed, with the firm claiming its billing model is up to two-thirds cheaper than some competitors.

Revenue is not publicly disclosed, no funding rounds have been recorded, and the company is privately held with no parent organisation. Publicly named represented organisations include Tauropharm, Medcomp, Heraeus, and Kirwan. The company is actively recruiting additional regulatory and quality professionals on flexible and fractional terms, suggesting a measured approach to capacity expansion. The technology stack is minimal — a content website and standard contact channels — with no app, no API, no AI capabilities, and no disclosed software products.

Short descriptiontext

MPS Medical-Product-Service UK Ltd is a Devizes-based regulatory consulting firm providing UK Responsible Person, EU MDR EC-REP, and US local representative services to international medical device manufacturers seeking multi-territory regulatory clearance.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersDevizes, United Kingdom
HQ citystring
Devizes
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
medical device regulatory, UK Responsible Person, EU Authorised Representative, regulatory compliance consulting, international medical device compliance
Industry2 codes
PRIMARYHLAGAKAO
Third-Party/Outsourced Quality & Responsible Person Services (EU QP/RP, US Agent)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Regulatory Affairs, Quality & Compliance Services (GxP)
SECONDARYHLAGAKAF
Inspection Readiness & Regulatory Authority Support (FDA/EMA/MHRA)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Regulatory Affairs, Quality & Compliance Services (GxP)
Product category
Medical Device Regulatory Consulting
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Regulatory Consulting Services
TypeProfessional Services
Description

Professional consulting services for medical device regulatory strategy, quality management system development, and compliance support across UK, EU, and USA markets.

mps-uk.uk
Marketing channels2 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Personnel, Operations, Marketing or Sales, Others
Pricing details1 tier
1Quote-based professional services
ModelOtherBilling cadenceMulti-year contract
Notes

Pricing not publicly disclosed; consultation and service fees determined based on client requirements and scope of engagement.

mps-uk.uk
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

MPS Medical-Product-Service UK Ltd provides regulatory representative and compliance services for international medical device manufacturers. Its core offerings include UK Responsible Person services under UK MHRA requirements, EU EC-REP (Authorised Representative) services under EU MDR, and US Local Representative support for FDA interactions. The firm serves as the in-country regulatory point of contact between non-UK/EU/US manufacturers and the competent authorities in those markets.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • Up to two thirds cheaper than some competitors
Product overview1 text field

MPS Medical-Product-Service (UK) Ltd is a regulatory consulting firm offering a unified suite of services for international medical device companies. The core offering comprises UK Medical Device Responsible Person Services (MHRA registration), EU MDR EC-REP Services, International Regulatory and Quality Consulting, Medical Device Clearance Consulting, and Medical Device Local Representation services across the UK, EU, and USA. These services work together to provide comprehensive regulatory support from early-stage university spin-outs through to full market clearance and ongoing compliance management.

Product and service4 records
1UK Responsible Person Service
CategoryRegulatory Representative Services
Description

Acts as the mandated UK Responsible Person for non-UK medical device manufacturers, serving as the regulatory point of contact with the MHRA and ensuring post-market compliance under UK medical device regulations.

2EU Authorised Representative (EC-REP) Service
CategoryRegulatory Representative Services
Description

Provides EU Authorised Representative (EC-REP) services under EU MDR for non-EU medical device manufacturers, including liaison with EU competent authorities and regulatory compliance support.

3US Local Representative Service
CategoryRegulatory Representative Services
Description

Acts as the US Local Representative for international medical device manufacturers needing a US-based point of contact for FDA interactions and US regulatory compliance.

4Medical Device Regulatory Consulting
CategoryRegulatory Consulting
Description

Advisory and consulting services supporting medical device manufacturers with regulatory strategy, compliance documentation, and cross-jurisdictional market access planning.

Scale indicator1 record

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

MPS represents Tauropharm as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

MPS represents Medcomp as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

MPS represents Heraeus as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

MPS represents Kirwan as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Parent/affiliated company enabling MPS UK to provide EU MDR EC-REP services. Through this partnership, MPS can help clients comply with EU Medical Device Regulations and the need for an EC-REP.

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Medical device and pharmaceutical regulatory compliance and quality consulting firm providing EU AR, US Agent, QMS implementation, and regulatory strategy — substantially overlapping with MPS's service line, particularly for SMEs and start-ups.

TypeDirect peer
Description

US-based medical device regulatory and quality consulting firm offering FDA submission, EU AR, and Quality System support — competing with MPS for the same international medical device manufacturer segment.

TypeDirect peer
Description

Global regulatory consulting and outsourcing firm with dedicated medical device regulatory services spanning US, EU, and UK — competing head-to-head with MPS for international medical device clients needing multi-market representation and submission support.

TypeDirect peer
Description

Specialised medical device regulatory affairs and quality consulting firm headquartered in Switzerland, providing EU AR services, MDR/IVDR transition support, clinical evaluation, and QMS development — overlapping with MPS's core EU-facing capabilities.

TypeBroad incumbent
Description

Medical-focused CRO and regulatory consulting organisation offering regulatory strategy, clinical evaluation, and quality services for medical devices — a broader incumbent that intersects with MPS's regulatory strategy and submission work.

TypeDirect peer
Description

One of the largest independent medical device and IVD regulatory and quality consulting firms, offering RA/QA strategy, Notified Body readiness, US Agent, EU AR, and UK RP services — directly overlapping with MPS's full service portfolio across all three major regulatory regimes.

TypeBroad incumbent
Description

Global testing, certification, and notified body group offering medical device regulatory services including EU AR, MDSAP, and CE marking support — a broad incumbent that competes with MPS for regulatory consulting engagements, though within a much larger portfolio.

TypeBroad incumbent
Description

Global CRO with significant medical device and regulatory services capability — a broad incumbent that competes for larger medical device regulatory and clinical consulting engagements that are adjacent to MPS's territory.

TypeBroad incumbent
Description

UK-headquartered standards, certification, and notified body organisation that interacts with medical device manufacturers on the same MDR/UKCA pathway MPS supports — a much larger incumbent whose regulatory and conformity services partly overlap with MPS's offering.

TypeBroad incumbent
Description

International testing, inspection, and certification organisation with medical device regulatory and notified body services — a broad incumbent whose medical device regulatory consulting overlaps with MPS in EU and US markets.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

MPS Medical-Product-Service UK Ltd

Medical Device Regulatory Consultingmps-uk.uk

MPS Medical-Product-Service UK Ltd is a Devizes-based regulatory consulting firm providing UK Responsible Person, EU MDR EC-REP, and US local representative services to international medical device manufacturers seeking multi-territory regulatory clearance.

What MPS Medical-Product-Service UK Ltd does

MPS Medical-Product-Service UK Ltd is a regulatory consulting firm headquartered in Devizes, Wiltshire, United Kingdom, founded in 2021. The company provides three core services to international medical device manufacturers: (1) UK Medical Device Responsible Person services, registering and maintaining devices with the MHRA; (2) EU MDR EC-REP services delivered through an affiliated German entity, MPS GMBH; and (3) US local representative services. The firm also develops tailored regulatory strategies and Quality Management Systems, and prepares Technical Files and Clinical Evaluation Filings for clearance across UK, EU, and USA markets. Its primary customer segment is international medical device companies, with secondary engagement from university spin-outs and start-ups requiring early-stage regulatory guidance.

The business operates as a low-overhead, relationship-driven professional services firm with a team of six, including three regional engagement leads (Ben Wensley-Stock for the UK, Gerhard Frömel for the EU, Reuben Lawson for the USA) each bringing 25-30 years of medical device industry experience. The go-to-market is direct and consulting-led, with the company's website as the primary marketing channel and direct contact (email and telephone) as the bottom-of-funnel conversion method. There is no proprietary software platform; the offering is entirely human-expertise-based. Pricing is quote-based and not publicly disclosed, with the firm claiming its billing model is up to two-thirds cheaper than some competitors.

Revenue is not publicly disclosed, no funding rounds have been recorded, and the company is privately held with no parent organisation. Publicly named represented organisations include Tauropharm, Medcomp, Heraeus, and Kirwan. The company is actively recruiting additional regulatory and quality professionals on flexible and fractional terms, suggesting a measured approach to capacity expansion. The technology stack is minimal — a content website and standard contact channels — with no app, no API, no AI capabilities, and no disclosed software products.

MPS Medical-Product-Service UK Ltd firmographics

Firmographics
Name
MPS Medical-Product-Service UK Ltd
Legal name
MPS Medical-Product-Service (UK) Ltd
Website
https://mps-uk.uk
Company type
Private
Operating status
Operating
Headcount range
1–10 employees
Short description
MPS Medical-Product-Service UK Ltd is a Devizes-based regulatory consulting firm providing UK Responsible Person, EU MDR EC-REP, and US local representative services to international medical device manufacturers seeking multi-territory regulatory clearance.
Ownership category
akta.pro rank

MPS Medical-Product-Service UK Ltd industry classification

Industry
Product category
Medical Device Regulatory Consulting
akta.pro industry
PRIMARYHLAGAKAO
Third-Party/Outsourced Quality & Responsible Person Services (EU QP/RP, US Agent)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Regulatory Affairs, Quality & Compliance Services (GxP)
SECONDARYHLAGAKAF
Inspection Readiness & Regulatory Authority Support (FDA/EMA/MHRA)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Regulatory Affairs, Quality & Compliance Services (GxP)

Keywords

  • Medical device regulatory
  • UK Responsible Person
  • EU Authorised Representative
  • Regulatory compliance consulting
  • International medical device compliance

Where MPS Medical-Product-Service UK Ltd is headquartered

Location

Headquarters

HQ city
Devizes
HQ country
United Kingdom
HQ region
Europe

Offices1 record

Markets served

MPS Medical-Product-Service UK Ltd business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Marketing or Sales, Others

Revenue model

  1. Regulatory Consulting Services: Professional consulting services for medical device regulatory strategy, quality management system development, and compliance support across UK, EU, and USA markets.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractQuote-based professional services

Go-to-market motion1 record

Distribution channels1 record

Marketing channels2 records

MPS Medical-Product-Service UK Ltd product offering

Product offering

Core offering

MPS Medical-Product-Service UK Ltd provides regulatory representative and compliance services for international medical device manufacturers. Its core offerings include UK Responsible Person services under UK MHRA requirements, EU EC-REP (Authorised Representative) services under EU MDR, and US Local Representative support for FDA interactions. The firm serves as the in-country regulatory point of contact between non-UK/EU/US manufacturers and the competent authorities in those markets.

Product overview

MPS Medical-Product-Service (UK) Ltd is a regulatory consulting firm offering a unified suite of services for international medical device companies. The core offering comprises UK Medical Device Responsible Person Services (MHRA registration), EU MDR EC-REP Services, International Regulatory and Quality Consulting, Medical Device Clearance Consulting, and Medical Device Local Representation services across the UK, EU, and USA. These services work together to provide comprehensive regulatory support from early-stage university spin-outs through to full market clearance and ongoing compliance management.

Differentiator

Problem solved

Functional benefit

Products and services

  • UK Responsible Person Service Acts as the mandated UK Responsible Person for non-UK medical device manufacturers, serving as the regulatory point of contact with the MHRA and ensuring post-market compliance under UK medical device regulations.
  • EU Authorised Representative (EC-REP) Service Provides EU Authorised Representative (EC-REP) services under EU MDR for non-EU medical device manufacturers, including liaison with EU competent authorities and regulatory compliance support.
  • US Local Representative Service Acts as the US Local Representative for international medical device manufacturers needing a US-based point of contact for FDA interactions and US regulatory compliance.
  • Medical Device Regulatory Consulting Advisory and consulting services supporting medical device manufacturers with regulatory strategy, compliance documentation, and cross-jurisdictional market access planning.

Quantifiable outcome

  • Up to two thirds cheaper than some competitors

Companies that use MPS Medical-Product-Service UK Ltd

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles1 record

MPS Medical-Product-Service UK Ltd technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

MPS Medical-Product-Service UK Ltd partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered core.

  • TauropharmcoreStrategic or Co-development PartnerMPS represents Tauropharm as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.
  • MedcompcoreStrategic or Co-development PartnerMPS represents Medcomp as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.
  • HeraeuscoreStrategic or Co-development PartnerMPS represents Heraeus as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.
  • KirwancoreStrategic or Co-development PartnerMPS represents Kirwan as their UK local representative organisation, providing regulatory and compliance services for their medical devices in the UK market.
  • MPS GMBH (Germany)coreStrategic or Co-development PartnerParent/affiliated company enabling MPS UK to provide EU MDR EC-REP services. Through this partnership, MPS can help clients comply with EU Medical Device Regulations and the need for an EC-REP.

Scale indicators1 record

Recent moves5 records

Expansion highlights4 records

MPS Medical-Product-Service UK Ltd competitors and assessment

Company assessment

Direct peers

  • Maetrics: Medical device and pharmaceutical regulatory compliance and quality consulting firm providing EU AR, US Agent, QMS implementation, and regulatory strategy — substantially overlapping with MPS's service line, particularly for SMEs and start-ups.
  • Kapstone Medical: US-based medical device regulatory and quality consulting firm offering FDA submission, EU AR, and Quality System support — competing with MPS for the same international medical device manufacturer segment.
  • Freyr Solutions: Global regulatory consulting and outsourcing firm with dedicated medical device regulatory services spanning US, EU, and UK — competing head-to-head with MPS for international medical device clients needing multi-market representation and submission support.
  • Medidee: Specialised medical device regulatory affairs and quality consulting firm headquartered in Switzerland, providing EU AR services, MDR/IVDR transition support, clinical evaluation, and QMS development — overlapping with MPS's core EU-facing capabilities.
  • RQM+: One of the largest independent medical device and IVD regulatory and quality consulting firms, offering RA/QA strategy, Notified Body readiness, US Agent, EU AR, and UK RP services — directly overlapping with MPS's full service portfolio across all three major regulatory regimes.

Broad incumbents

  • NAMSA: Medical-focused CRO and regulatory consulting organisation offering regulatory strategy, clinical evaluation, and quality services for medical devices — a broader incumbent that intersects with MPS's regulatory strategy and submission work.
  • TÜV SÜD: Global testing, certification, and notified body group offering medical device regulatory services including EU AR, MDSAP, and CE marking support — a broad incumbent that competes with MPS for regulatory consulting engagements, though within a much larger portfolio.
  • ICON plc: Global CRO with significant medical device and regulatory services capability — a broad incumbent that competes for larger medical device regulatory and clinical consulting engagements that are adjacent to MPS's territory.
  • BSI Group: UK-headquartered standards, certification, and notified body organisation that interacts with medical device manufacturers on the same MDR/UKCA pathway MPS supports — a much larger incumbent whose regulatory and conformity services partly overlap with MPS's offering.
  • DEKRA: International testing, inspection, and certification organisation with medical device regulatory and notified body services — a broad incumbent whose medical device regulatory consulting overlaps with MPS in EU and US markets.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat3 records

Key risks5 records

Key highlights5 records

Customer concentration

MPS Medical-Product-Service UK Ltd social profiles

Digital presence

MPS Medical-Product-Service UK Ltd financial estimates

Financial estimate

Revenue estimate

Valuation estimate

MPS Medical-Product-Service UK Ltd leadership team

Management profile

Number of profiles

Profiles3 records

MPS Medical-Product-Service UK Ltd funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

MPS Medical-Product-Service UK Ltd M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about MPS Medical-Product-Service UK Ltd

What does MPS Medical-Product-Service UK Ltd do?

MPS Medical-Product-Service UK Ltd provides regulatory representative and compliance services for international medical device manufacturers. Its core offerings include UK Responsible Person services under UK MHRA requirements, EU EC-REP (Authorised Representative) services under EU MDR, and US Local Representative support for FDA interactions. The firm serves as the in-country regulatory point of contact between non-UK/EU/US manufacturers and the competent authorities in those markets.

Is MPS Medical-Product-Service UK Ltd a public or private company?

MPS Medical-Product-Service UK Ltd is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was MPS Medical-Product-Service UK Ltd founded?

MPS Medical-Product-Service UK Ltd was founded in -1. It employs 1 to 10 people.

Where is MPS Medical-Product-Service UK Ltd based?

MPS Medical-Product-Service UK Ltd is headquartered in Devizes, United Kingdom, in the Europe region.

How does MPS Medical-Product-Service UK Ltd make money?

One revenue line is on record: regulatory Consulting Services.

Who are MPS Medical-Product-Service UK Ltd's main competitors?

Direct peers on record are Maetrics, Kapstone Medical, Freyr Solutions, Medidee and RQM+. Broad incumbents are NAMSA, TÜV SÜD, ICON plc, BSI Group and DEKRA.

Does MPS Medical-Product-Service UK Ltd have an API?

No public API is recorded for MPS Medical-Product-Service UK Ltd.

What industry is MPS Medical-Product-Service UK Ltd in?

MPS Medical-Product-Service UK Ltd's product category is Medical Device Regulatory Consulting. Its primary akta.pro industry code is HLAGAKAO, Third-Party/Outsourced Quality & Responsible Person Services (EU QP/RP, US Agent), with a secondary code of HLAGAKAF, Inspection Readiness & Regulatory Authority Support (FDA/EMA/MHRA).

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