Is Medical Device (MD) and In-Vitro Diagnostics (IVD) cybersecurity compliance hard to understand? Do you wonder how it fits in with all the rest of MD and IVD development and release processes? At Qserve, we often encounter clients who struggle during submission time trying to react to questions and requests from regulatory bodies for cybersecurity evidence.
In this webinar we will explain why cybersecurity is much more than a “tack-on” item. We will provide context and a comprehensive cybersecurity view to medical and in-vitro medical devices. The goal is to motivate a thorough proactive cybersecurity process in MD and IVD development.
Key takeaways include:
- How cybersecurity aligns with software development process and deliverables
- How cybersecurity aligns with risk management
- What are the expectations in maintaining cybersecurity post-market?
Watch the Webinar On-Demand by clicking the link below,