UK Market Access Partners (UKRP)

UK Market Access Partners

UK Market Access Partners (UKRP) provides expert medical device lifecycle management services, including UK Responsible Person (UKRP) services for manufacturers outside the UK.

UK Market Access Partners (UKRP) offers comprehensive medical device lifecycle management, guiding manufacturers from concept and design through to market access and post-market surveillance. They specialize in ensuring compliance and audit readiness for MedTech and BioTech companies of all sizes. A key service is acting as the UK Responsible Person (UKRP), a mandatory requirement for non-UK-based manufacturers wishing to place medical devices on the Great Britain market, as stipulated by the UK Medical Devices Regulation 2002. UKRP facilitates smoother market entry and ongoing compliance for international clients. Evnia, the entity behind UK Market Access Partners, leverages industry knowledge and proprietary tools to transform challenges into opportunities. They help clients shorten time-to-market and support day-to-day business operations both pre- and post-market. Their services are tailored to the unique needs of each medical product, adding clinical and commercial value to portfolios and enabling companies to take their innovations to international markets faster and with less risk.

About

**Who they are**
UK Market Access Partners (UKRP) provides expert medical device lifecycle management services, including UK Responsible Person (UKRP) services for manufacturers outside the UK.

**Expertise & scope**
* Specializes in UK Responsible Person (UKRP) services.
* Supports medical device manufacturers needing representation in the UK.
* Offers comprehensive medical device lifecycle management.

**Reputation / proof points**
* Established presence in the UK market.

Additional information

UK Market Access Partners (UKRP) focuses on ensuring medical devices comply with UK regulations. Their UKRP service is crucial for overseas manufacturers looking to place their products on the Great Britain market. This service acts as a point of contact for regulatory authorities and ensures ongoing compliance with relevant legislation. Buyers should consider the scope of lifecycle management services offered, which can extend beyond the basic UKRP role to encompass broader regulatory strategy and support.

Key Highlights

  • Provides UK Responsible Person (UKRP) services for non-UK manufacturers. Source
    “UK Market Access Partners (UKRP) provides expert medical device lifecycle management services, including UK Responsible Person (UKRP) services for manufacturers outside the UK.”
  • Offers expert medical device lifecycle management. Source
    “UK Market Access Partners (UKRP) provides expert medical device lifecycle management services, including UK Responsible Person (UKRP) services for manufacturers outside the UK.”

Certifications & Trust Signals

  • Operates within the UK regulatory framework. Source
    “UK Market Access Partners (UKRP) provides expert medical device lifecycle management services, including UK Responsible Person (UKRP) services for manufacturers outside the UK.”

Buyer Snapshot

Best for
  • Manufacturers outside the UK seeking UK Responsible Person services
  • Companies requiring medical device lifecycle management
How engagement typically works
  • Retainer-based UKRP services
  • Project-based lifecycle management
Typical deliverables
  • UK Responsible Person designation
  • Regulatory compliance support for the UK market
  • Lifecycle management strategy
Good to know
  • Best when the primary need is UK market access and regulatory representation.
HQ: Manchester, UK
Languages: English
Timezones: Europe/London
Status: listed

Services & Capabilities

Best UK Responsible Person (UKRP) | Compare & Get Quotes

Jurisdictions: UK
Countries: GB
Industries: Medical devices, IVD, Healthcare
Portfolio: 6-25, 26-100
Onboarding time: 3–21 days
Pricing model: Onboarding + annual retainer
Starting from: GBP 3,200
Included services: UK Responsible Person (UKRP) designation, MHRA liaison and communications forwarding, Support for registration process readiness, Vigilance escalation workflows and FSCA coordination, Labeling check for UKRP identification
Supports GB: Yes
MHRA Support: Yes
Can Be Named On Label: Yes
Vigilance Support: Yes

Additional uk_rp Details

Supports MDR
true
Supports GB
true
Vigilance Support
true
Post Market Support
true
UK Entity Country
England
Onboarding Steps
Requires detailed information about the medical device, including classification and intended use, to facilitate appointment and ongoing support.
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