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Given the high-stakes nature of medical devices, safety, compliance, and speed are central concerns for medical device developers. Therefore, tools and solutions that define requirements, mitigate risk, guide compliance, avoid errors and streamline the development process are such valuable resources.

In this guide, explore how MedTech companies can better manage risk and speed time to market, understand FMEA vs. ISO 14971, and learn how to properly balance risks and requirements.

Vendor:

Jama Software

Posted:

Feb 8, 2021

Published:

Dec 17, 2020

Format:

PDF

Type:

White Paper