Medical Devices: Sources of Regulation (Ireland)

Life Sciences Partners Michaela Herron and James Gallagher authored a guide to Medical Devices: Sources of Regulation (Ireland) for Thomson Reuters Practical Law.

The chapter explains the regulatory regimes that apply to medical devices and their components in Ireland. It covers both regulatory regimes specific to medical devices and general regulatory regimes that apply to a range of products including medical devices.

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Reproduced from Practical Law with the permission of the publishers. For further information, visit www.practicallaw.com.