Helping medical device manufacturers stay in compliance with ISO quality standards and FDA regulations

March 21, 2017 Tektronix Experts

A recent meeting with a large medical device customer lead to an enlightening discussion on the differences between International Organization for Standardization (ISO) and US Food and Drug Administration (FDA) standards and regulations as they apply to medical device manufacturers. This is a short overview of a few of the key differences between ISO and FDA compliance and a quick guide to choosing a calibration provider that can help you build an ironclad calibration program.

  

Key Differences Between FDA Regulations and ISO Standards

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