The Medical Device Software Development Summit

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

URLs:

Tickets: https://go.evvnt.com/1514112-1?pid=5248

Brochure: https://go.evvnt.com/1514112-3?pid=5248

Prices:

Standard Pricing - Conference Only: USD 2999.00,

Standard Pricing - Conference + Workshop Day: USD 4395.00,

Vendor Pricing - Conference Only: USD 3599.00,

Academic Pricing - Conference Only: USD 2599.00,

Academic Pricing - Conference + Workshop Day: USD 3995.00

Speakers: Anthony Watson, Vice President - Regulatory Affairs and Quality, Pear Therapeutics, Bemin Ghobreal, R and D Software Engineering Manager - Surgical Robotics, Medtronic, Cabell Maddux, Director of Engineering, Day Zero Diagnostics Inc., Caroline Kirwan, Director of Regulatory Affairs and Quality, Cumulus Neuroscience, Chris Puryear, Vice President, Engineering, Bigfoot Biomedical Inc., Gregg Harris, Vice President Clinical/Regulatory, VisCardia Inc., Gregory Stern, Director of Product (SaMD), Insulet Corporation, Jennifer Newberger, Vice President and Head of Regulatory and Compliance, Cognito Therapeutics Inc., John Beebe, Surgical Robotics and Quality Systems Manager, Medtronic, Ken Tubman, Director, Connected and Software Devices, Takeda, Khaudeja Bano, MD, Vice President - Combination Product Quality, Amgen Inc., Lesley Butler, Head of RWE Digital Innovation, UCB S.A., Lynda Jeffcoat, Director, Software Lifecycle, Alcon, Mark Lifson, Director, Artificial Intelligence Systems Engineering, Mayo Clinic, Oleg Yusim, Head of Product Security, Edwards Lifesciences, Pat Baird, Head Of Global Regulatory and Software, Philips, Randy Horton, Co-Chair of Cloud Working Group and Technical Information Report, AAMI, Robert Ezzell, Senior Director, Regulatory Affairs, ATAI Life Sciences, Sameer Jaiswal, Director, Abbott Rapid Diagnostics QARA, Digital and eServices, Abbott Laboratories, Sunny Webb, Chief Technical Officer, Verisk Health, Tapani Otala, Vice President of Engineering, Tidepool, Uma Chandrashekhar, Global Information Product Security Officer, Alcon, Venk Varadan, CEO and Co-founder, Nanowear, Inc., Xenophon (Xenios) Papademetris, Professor, Yale University School of Medicine

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