2017 Medical Devices Manufacturers Software Selection Guide

Today, the challenges Medical Device companies encounter are expanding. The FDA’s “Case for Quality” calls for manufacturers to ensure the highest levels of device quality and safety throughout product design, manufacture and service. As a result, teams need to consider comprehensive closed looped solutions.

By including all disciplines into the product lifecycle from design, teams can avoid unnecessary iterations and rework while adhering to complex compliance regulations. This independent  guide identifies the critical challenges, key capabilities, and vendor selection criteria to help you select the right technology and partner to meet your needs.

Preview The Medical Devices Manufacturers Software Selection Guide Table of Contents And Executive Overview


Michelle Boucher is the Vice President of Research for Tech-Clarity. Michelle has spent over 20 years in various roles in engineering, marketing, management, and as an analyst. She has broad experience with topics such as product design, simulation, systems engineering, mechatronics, embedded systems, PCB design, improving product performance, process improvement, and mass customization. Ms. Boucher is an experienced researcher and author and has benchmarked over 7000 product development professionals and published over 90 reports on product development best practices. She focuses on helping companies manage the complexity of today’s products, markets, design environments, and value chains to achieve higher profitability.