Medical Device Premarket and Post market Cyber security following the new FDA Guidances 2017 is a webinar that covers topics such as:
- Current cybersecurity threats to medical devices
- What is cybersecurity
- Developing robust security mitigations to incorporate into your device design
- FDA`s perspectives on the roles of medical device suppliers in cybersecurity management
- Cybersecurity risk analysis
- How to maintain a compliant program
- Interfacing with network users
- Information sharing groups(ISAO)
- FDA conditions for not reporting cybersecurity problems
Medical Device Premarket and Post market Cyber security following the new FDA Guidances 2017 is intended for:
- Hospital Risk Managers
- Medical device company CEOs/Presidents/Managing Directors
- IT security professionals
- Clinical Department Heads
- Regulatory Personnel
- Engineering Manager
- Production Management
- Development Engineers
- Software Developers
- QA/QC Personnel
- Risk managers
- Usability engineers
- Design Engineering Managers
