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) offers specialized UK Responsible Person (UKRP) services, alongside QA/RA consulting and training, primarily for the medical device and pharmaceutical sectors. They focus on ensuring regulatory compliance and supporting business development.
**Expertise & scope**
* UK Responsible Person (UKRP) services
* Quality Assurance (QA) and Regulatory Affairs (RA) consulting
* QA/RA training services
* ISO 13485 Quality Management Systems support and implementation
* Support for UK medical device regulatory requirements
* Guidance on MDR and IVDR requirements
* ISO Audit Support
* Environmental / CSR Services
**Reputation / proof points**
* Tim Briffitt has 20 years of experience across the medical devices and pharmaceutical sectors, with a focus on UK medical device regulatory requirements for the last 2 years.
Libera Voce (UKRP) offers specialized UK Responsible Person (UKRP) services, alongside QA/RA consulting and training, primarily for the medical device and pharmaceutical sectors. They focus on ensuring regulatory compliance and supporting business development.
**Expertise & scope**
* UK Responsible Person (UKRP) services
* Quality Assurance (QA) and Regulatory Affairs (RA) consulting
* QA/RA training services
* ISO 13485 Quality Management Systems support and implementation
* Support for UK medical device regulatory requirements
* Guidance on MDR and IVDR requirements
* ISO Audit Support
* Environmental / CSR Services
**Reputation / proof points**
* Tim Briffitt has 20 years of experience across the medical devices and pharmaceutical sectors, with a focus on UK medical device regulatory requirements for the last 2 years.
Additional information
Libera Voce Consulting aims to create work placements through its growing operations, generating employment opportunities for individuals seeking flexible, remote work. This initiative reflects a commitment to social responsibility alongside their core regulatory services. Their approach to QA/RA consulting and training is tailored to meet the specific needs of clients in the medical device and pharmaceutical industries, ensuring a practical and compliant path to market.
Key Highlights
-
Tim Briffitt brings 20 years of experience in medical devices and pharmaceuticals, with the last 2 years focused on UK medical device 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.”
-
Offers specialized services including UK Responsible Person (UKRP) functions, QA/RA consulting, and training.
Source
“UKRP Services QA / RA Consulting QA / RA Training Services”
-
Provides support for ISO 13485 Quality Management Systems, including optimization and implementation.
Source
“He has optimised and implemented processes and training on: ISO13485 Quality Management Systems”
-
Services cover UK medical device regulatory requirements, MDR, IVDR, and ISO audit support.
Source
“UKRP activities MDR requirements IVDR requirements ISO Audit Support”
Certifications & Trust Signals
-
Established presence with specific expertise in UK medical device regulations.
Source
“In the last 2 years, he has focused his skills on UK medical device regulatory requirements.”
Buyer Snapshot
Best for
- Medical device and pharmaceutical companies requiring UKRP services
- Businesses needing tailored QA/RA consulting and training
- Organizations seeking ISO 13485 implementation support
How engagement typically works
- Bespoke service delivery
- Focus on regulatory compliance and business development
- Provision of training and consulting
Typical deliverables
- UKRP designation and support
- Optimized regulatory processes
- ISO 13485 compliant systems
- Training materials and sessions
- Audit support
Good to know
- Best when focused on UK medical device and pharmaceutical sectors
HQ:
Reading, 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:
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
true
Supports IVDR
true
Supports GB
true
UK Entity Country
England
