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TIM BRIFFITT
UKRP QUALITY DIRECTOR
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. He has optimised and implemented processes and training on:
UKRP activities
MDR requirements
IVDR requirements
ISO13485 Quality Management Systems
ISO13485:2016 Transition
Notified Body Transfer
ADMIN SUPPORT
Your first contact ...
To support the work of the directors, ad hoc administrational support has been brought in from a local CIC.
As the work grows, we are aiming to create work placements to generate employment for people who find it difficult to access flexible, remote opportunities.
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