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Understanding the Clinical Evidence of the EU IVDR Webinar
Автор: RegDesk
Загружено: 2025-10-29
Просмотров: 107
Описание:
The transition to the EU In Vitro Diagnostic Regulation (IVDR) continues to challenge manufacturers and regulatory teams worldwide. From new classification rules to increased performance evaluation requirements, staying compliant under the IVDR demands both precision and preparation.
In this webinar, RegDesk brings expert Lee Westwood, an industry leader with deep experience in EU regulatory frameworks, to break down what companies need to do now to meet IVDR requirements and avoid costly delays.
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