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European Handbook of Medical Devices Regulatory Affairs 2025

Publisher Asia Pacific InfoServe (API)
Published Jan 25, 2025
Length 200 Pages
SKU # API19509753

Description

European Handbook of Medical Devices Regulatory Affairs 2025


This Handbook is an excellent reference for understanding what is required to bring medical devices to European markets under the many different regulatory systems. It begins by providing concepts such as device classification, clinical trials, & labelling.

Table of Contents

200 Pages
Please Note: Due to the brevity and/or nature of the content posted, there is no table of contents available for this report.

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