Libera Voce (UKRP)

Libera Voce Consulting

Libera Voce Consulting offers bespoke UK Responsible Person (UKRP) services, specializing in Quality Assurance (QA), Regulatory Affairs (RA), and comprehensive business development. They cater to the medical device and pharmaceutical sectors, focusing on ensuring regulatory compliance and fostering business growth. Their approach is 'made to measure,' meaning they tailor their consulting services, including organizational development, audits, and mentoring, to the specific needs of each client.

Libera Voce Consulting provides specialized UK Responsible Person (UKRP) services, focusing on Quality Assurance (QA) and Regulatory Affairs (RA) for businesses in the medical device and pharmaceutical industries. Established to bring order and strategic development to organizations, they offer made-to-measure consulting, audits, and mentoring. With expertise in MDR and IVDR requirements, ISO13485 Quality Management Systems, and ISO13485:2016 transitions, Libera Voce supports clients in navigating complex regulatory landscapes. Their services extend to QA/RA training, ISO audit support, and environmental/CSR services. The team, including Tim Briffitt with 20 years of experience, is dedicated to optimizing processes and ensuring compliance. Libera Voce is committed to client needs, offering a bespoke approach to business development and regulatory challenges. They also aim to create employment opportunities through work placements for individuals seeking flexible, remote roles.

About

**Who they are**
Libera Voce (UKRP) provides bespoke UK Responsible Person services, specializing in Quality Assurance (QA) and Regulatory Affairs (RA) for the medical device and pharmaceutical sectors. They focus on ensuring regulatory compliance and fostering business growth through tailored consulting.

**Expertise & scope**
* UK Responsible Person (UKRP) services
* Quality Assurance (QA) and Regulatory Affairs (RA) consulting
* QA / RA Training Services
* ISO Audit Support, including ISO 13485 Quality Management Systems
* Support for MDR and IVDR requirements
* Environmental / CSR Services
* Organizational development, audits, and mentoring
* Tailored 'made to measure' consulting approach

**Reputation / proof points**
* Tim Briffitt has 20 years of experience in the medical devices and pharmaceutical sectors, with a recent focus on UK medical device regulatory requirements.
* Focus on creating work placements to generate employment opportunities.

Additional information

Libera Voce Consulting emphasizes a 'made to measure' approach, ensuring their services are customized to the unique needs of each client. This includes bespoke consulting for organizational development, audits, and mentoring. Their expertise extends to critical regulatory frameworks such as the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), alongside ISO 13485 Quality Management Systems. They also offer support for environmental and Corporate Social Responsibility (CSR) initiatives, demonstrating a holistic approach to business compliance and growth.

Key Highlights

  • Specializes in bespoke UK Responsible Person (UKRP) services. Source
    “Libera Voce Consulting offers bespoke UK Responsible Person (UKRP) services”
  • Offers expertise in Quality Assurance (QA), Regulatory Affairs (RA), and business development. Source
    “specializing in Quality Assurance (QA), Regulatory Affairs (RA), and comprehensive business development.”
  • Provides tailored consulting, including organizational development, audits, and mentoring. Source
    “tailor their consulting services, including organizational development, audits, and mentoring”
  • Supports compliance with MDR and IVDR requirements. Source
    “MDR requirements IVDR requirements”
  • Tim Briffitt brings 20 years of experience in medical devices and pharmaceuticals, focusing on UK regulatory requirements. Source
    “Tim joined Libera Voce in 2022 with 20 years of experience from across the medical devices and pharmaceutical sectors. In the last 2 years, he has focused his skills on UK medical device regulatory requirements.”

Certifications & Trust Signals

  • Focuses on ISO 13485 Quality Management Systems. Source
    “ISO13485 Quality Management Systems”

Buyer Snapshot

Best for
  • Medical device and pharmaceutical companies needing UKRP services
  • Businesses seeking tailored QA/RA consulting
  • Companies requiring support with MDR and IVDR compliance
How engagement typically works
  • Bespoke, 'made to measure' consulting
  • Focus on organizational development and mentoring
  • Audit support and process optimization
Typical deliverables
  • UK Responsible Person designation
  • QA/RA strategy development
  • ISO 13485 implementation and audit support
  • Regulatory compliance guidance (MDR, IVDR)
Good to know
  • Best when clients require a highly customized approach to regulatory affairs and quality assurance.
HQ: Reading, UK
Languages: English
Timezones: Europe/London
Claim status: Listed

Services & Capabilities

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

Jurisdictions: UK
Countries: GB
Industries: Medical devices, IVD, Healthcare
Portfolio: 1-5, 6-25
Onboarding time: 3–21 days
Pricing model: Retainer
Starting from: GBP 2,000
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
Supports NI: No
MHRA Support: Yes
Can Be Named On Label: No
MHRA Portal Support: No
Vigilance Support: Yes

Additional uk_rp Details

Supports MDR
Yes
Supports IVDR
Yes
Supports GB
Yes
UK Entity Country
England
Vigilance Support
No
Post Market Support
No
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