The MEDevice Conference

Your all-access pass to regulatory strategy, emerging technology, and commercial growth.

#MEDeviceBoston

Built for the Teams Navigating MedTech's Toughest Challenges

The MEDevice Conference is a focused, expert-led program built around the specific challenges facing engineers, R&D teams, and growth-stage companies today. Master regulatory strategy, emerging technology, and commercialization, covered in depth by the people who know them best.

SAVE THE DATE

Why Attend the MEDevice Conference

All the strategies and updates engineered to help you upgrade your devices, stay compliant, and scale your operations.

Regulatory Readiness
Practical guidance on the FDA expectations and regulatory shifts impacting your work right now.
Technical Learning
Content built for engineers and R&D professionals, not general audiences.
Practical Takeaways
Actionable strategies you can bring back to your team the same week.
Future-Forward Perspective
Discover where MedTech is heading before it gets there.
Growth & Investment Insight
Learn how regulatory milestones and commercialization strategy impact valuation and long-term growth.

Three Tracks Covering the Challenges That Matter Most

Regulatory Update

Built to help you navigate a more complex and demanding regulatory environment.

Topics Include:

Cybersecurity Submissions: From Guidance to Enforcement
Human Factors as a Regulatory Risk Mitigation Tool
Software as a Medical Device (SaMD) in Practice
510(k), De Novo, or Breakthrough? Choosing the Right Pathway

MedTech Technology

Covering the technologies defining the next generation of medical devices.

Topics Include:

Digital Twins in Device Development
Robotics & Image-Guided Systems
Advanced Materials & Next-Gen Polymers: Engineering for Performance and Sustainability
Wearables Moving Into Clinical-Grade Devices

Growth & Investment

Learn the commercial side of MedTech,covered in depth for teams planning their next stage of growth.

Topics Include:

Mergers & Acquisitions in MedTech: Positioning for Strategic Growth
Commercializing Your Medical Device: From Clearance to Market Success
Design Controls Without Killing Your Speed
What Investors Look for in MedTech Startups

Who Should Attend

Engineers + R&D Professionals

Biomedical Engineers
Design & Development Engineers
Software & Systems Engineers
R&D Leaders and Program Managers

Regulatory & Quality Professionals

Regulatory Affairs Specialists
Quality Assurance and QMS Managers
Compliance Officers
Testing and Validation Leads

Business & Growth Leaders

Executives and Founders
Product and Program Managers
Business Development Professionals
Investors and Innovation Partners

Who You'll Meet

The people advancing medical device development in New England, all in one room.

OEM Leaders and Decision Makers
Executives, directors, and technical leads from New England's most influential medical device manufacturers.
Engineers and Innovators
Biomedical engineers, R&D specialists, and product designers building the next generation of medical devices.
Regulatory and Quality Experts
Compliance officers, QA managers, and regulatory affairs professionals keeping MedTech products safe and market-ready.

Everything Included With Your Conference Pass

Full Conference Access

Access to all three tracks and every session across both days.

Complimentary Refreshments

Enjoy coffee, drinks, and networking lunches throughout the conference.

Hands-On Workshops

Includes full access to every workshop. Workshops are also available a la carte through registration.

Expo Floor Access

200+ exhibitors, show floor education, the Innovation Lab, and all networking events.

VIEW PASSES & PRICING

2026 Call For Speakers! Submit Your Proposal — LEARN MORE