5th Medical Device Software Development Summit 2025

Date : 24th June 2025 to 26th June 2025

Place : United States of America, Boston

Website :https://medicaldevice-software-development.com/

Contact Person:Lauren Thursby

Description:

Benchmark and Fuse Knowledge from Software, QA, RA and Product Teams to Align Innovation in Software with Evolving Processes, Cybersecurity, and Global Regulatory Frameworks in New and Legacy Devices. Time: 8:00 AM - 3:10 PM.

5th Medical Device Software Development Summit 2025 will be held in Boston,United States of America on date 2025-06-26

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Deadline for abstracts/proposals : 24th June 2025

Keynote Speakers :

Conference Highlights :Home - 5th Medical Device Software Development Summit 2025
Join leading medical device manufacturers to tackle obstacles to design and develop software that is innovative, compliant, and secure. Hear exclusive case studies on MDR and FDA compliance, agile development methodologies, ISO standards for risk management, device usability design, AI, and cybersecurity.

Companies Already Confirmed to Attend:
The MedTech landscape is evolving rapidly, with FDA’s shifting expectations, AI-driven regulations, and global compliance challenges putting pressure on companies to innovate while maintaining security and compliance. With changing U.S. regulations, AI standards, and cybersecurity requirements, now is the time to ensure your team is prepared for these challenges. The5th Medical Device Software DevelopmentSummit offers the latest strategies to navigate these uncertainties and stay ahead in a complex, fast-paced industry.
The summit is designed for professionals across all functions- whether you're in software development, regulatory affairs, quality assurance, or cybersecurity. Through expert-led sessions and hands-on workshops, you'll gain actionable insights to tackle the latest challenges in AI integration, compliance, and development. No matter your role or organization size, this summit equips you with the knowledge and tools needed to drive innovation and navigate the complex MedTech landscape.
Unlock strategies to build resilient AI-cybersecurity frameworks amid regulatory uncertainty.OlympusandRetina AIwill reveal how to secure AI-driven medical devices, integrate cybersecurity into development, and stay ahead of evolving compliance demands.
Streamline global regulatory submissions across the FDA, EU, Japan, and beyond.Leaders fromAbbVieandAnalog Deviceswill share strategies to navigate complex approvals, harmonize multi-region submissions, and overcome cross-jurisdictional challenges with confidence.

Check the event website for more details.