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Overview of regulatory requirements for medical devices and IVDs: Part 2

Автор: HPRA Ireland

Загружено: 2025-06-09

Просмотров: 338

Описание: Nicola Hickie discusses regulatory considerations for Irish hospitals, covering system requirements, CE marking, post-2021 regulatory changes, and the roles of the HPRA and health institutions in implementing the Regulations.

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Overview of regulatory requirements for medical devices and IVDs: Part 2

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