Regulatory Lead
BSI, Belgium
Judith Prevoo is a Regulatory Lead for BSI The Netherlands Notified Body and she is responsible for the regulatory oversight of medical devices Notified Body strategy, policy, procedures and documentation to meet the various legislative and designation requirements. Before joining BSI in 2018, she gained over 13 years` experience in the In Vitro Diagnostic medical device and pharmaceuticals industries in both scientific and Quality Assurance roles.
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Companion Diagnostics: Overview of the IVDR Requirements and the EMA Consultation Process
Thursday, October 5, 2023
4:45 PM – 5:45 PM EDT