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Global Handbook of Medical Devices Regulatory Affairs 2025

Publisher Asia Pacific InfoServe (API)
Published Jan 25, 2025
Length 300 Pages
SKU # API19509752

Description

Global Handbook of Medical Devices Regulatory Affairs 2025


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

Table of Contents

300 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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