Multifunction Device Compliance
Regulatory, Risk & Cybersecurity Considerations
Join IZiel Healthcare for a technical webinar on developing and assessing multiple function device products, with a focus on FDA expectations and practical approaches to compliance.
Seven areas, each with a practical takeaway
The session works through the assessment the way a regulatory or engineering team would run it.
A practical, risk-based view of multifunction products
These products increasingly combine device functions, software, connectivity, cloud services and third-party technologies. Understanding how those functions interact is essential to an appropriate regulatory and risk-management strategy.
How to distinguish the medical device function from other functions in the same product.
How other functions may impact the safety and effectiveness of the device function.
Key considerations for software, cloud services, cybersecurity, interoperability and third-party components.
Practical considerations for regulatory assessment and supporting documentation.
Built for cross-functional teams
Multifunction assessments rarely sit with one department. The session is pitched for the people who have to agree on the answer.
Presented by IZiel Healthcare
Navigate the complexities of multifunction device compliance
Choose the session most convenient for your region.
We look forward to having you join us. — IZiel Healthcare
GALLERY
Preview of the Seminar conducted by IZiel along with their partners.
