Leveraging Periodic Post-Marketing Checks to Ensure Devices in Market Remain Compliant & Secure
Time: 9:45 am
day: Day One
Details:
- Reassessing the growing threat surface around this device from the time the device was launched into market
- Implementing continuous monitoring systems to ensure ongoing compliance and security of medical devices post-market
- Integrating post-market surveillance with 510(k) requirements to maintain FDA compliance through effective post-market evaluations
