The Medical Device Software Development Summit Hilton Boston Logan Airport, Boston

Designing Compliant, Innovative, and Secure Medical Device Software
Now in its 3rd year, this ambitious event unites software engineering, quality assurance and regulatory experts as well as regulatory bodies such as the GMED and hospital representatives to cover medical device software development challenges in a “lifecycle” manner sequentially covering agile development, usability, compliance, cybersecurity, risk analysis and testing.

Designed to be the only event you and your team need to attend in 2023, uncover 20+ case studies from manufacturers, notified bodies and regulatory authorities as they each provide a piece of the puzzle – enabling you to build your own roadmap to achieve regulatory compliance and innovative software design strategies.

Join 100+ leading device manufacturers, big pharma device teams and innovative startups as they utilize this rare and much needed opportunity to collaborate onand uncover solutions to their most pressing challenges including:

Overcoming the challenge of a fast-paced software world in a slow-paced regulatory world
Continuing to push the boundaries of innovation with AI-enabled medical devices
Employing risk analysis into the software development lifecycle to streamline a path to a secure and compliant device
Efficiently onboarding new software engineers with little experience in such a highly regulated landscape to ensure they are working effectively faster
Rethinking agile software development methodologies to be fit for purpose in 2023
Embedding cybersecurity across all layers of the medical devices development cycle to prevent breaches, warning letters and recalls