With FDA regulations limiting the kind of updates and protection tweaks you can make on medical devices, version control and patch management are important aspects of managing your clinical equipment risk condition.
Original Equipment Manufacturers (OEMs) release updates, upgrades and patches at varying intervals. eProtex manages this process for our customers, relieving you of the deep know-how and effort needed to manage these elements (and the dangers of managing them improperly).
We inform you of any new changes, assess the impact of each change, recommend strategies and manage the change process. We also document the entire consultative progression for your device records. Our watchful presence in this process gives you:
- Accurate, up-to-date visibility into device software options
- Recommendations consistent with your specific environment and security strategy
- Documentation for audit requirements and historical reference
