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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

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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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