FDA Medical Device Regulation Assessment

Are the FDA’s New Regulations on Medical Devices Making a Difference?

In 2023, the Food and Drug Administration (FDA) took a significant step in prioritizing medical device cybersecurity by issuing new requirements for premarket submission and ongoing monitoring. The goal was clear: to prevent cyberattacks that could put patients’ lives at risk. As we approach the one-year anniversary of these regulations, many are wondering – have they made a tangible impact?

Source: www.forbes.com