FDA 21 CFR 820 Compliance

Q & As Describe How FDA 21 CFR Part 820 Compliance and ISO 13485 Provide a Framework for Compliance for Meeting Medical Device Quality Standards and How to Prepare for FDA Inspections

Whether it's a simple thermometer or a sophisticated cardiac pacemaker, the goal of FDA 21 CFR Part 820 Compliance and ISO 13485 international standards is to ensure medical device quality and safety and to reduce, if not prevent, injuries and deaths. Learn how MasterControl's Quality Excellence can support your FDA 21 CFR Part 820 compliance efforts.

21 CFR Part 820 – ISO 13485 Harmonisation
Download