FDA 21 CFR Part 820 Quality System Regulation for Medical Devices

In This White Paper

We take a  closer look at the FDA 21 CFR Part 820 Quality System (QS) Regulation for medical devices and best practices to enable regulatory compliance.

“AssurX is the most flexible and intuitive solution on the market. It is also the most user-friendly from both the end user and administrative perspective. AssurX is 5–10 years ahead of their competitors.”

genzyme - FDA Part 820 Quality System Regulation for Medical Devices

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About AssurX:

With decades of expertise built into our quality management and regulatory compliance software platform, AssurX helps companies maintain quality and compliance, streamline workflow, control risks and better manage your enterprise. Our configurable software and deep understanding of users’ needs produce a unique system that easily adapts as your business evolves.

AssurX is an ideal partner for regulated companies looking for better operational control and efficiency while meeting and exceeding compliance standards.

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