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AUGUST 26 – 27, 2026
Thomas M. Menino Convention &
Exhibition Center (Formerly BCEC)
Boston, MA
AUGUST 26 – 27, 2026
Thomas M. Menino Convention &
Exhibition Center (Formerly BCEC)
Boston, MA
#MEDeviceBoston
From regulatory strategy and quality management systems to testing, sterilization, and packaging, MEDevice Boston brings together the experts and solution providers that keep medical device programs compliant, on schedule, and market-ready. Find the partners your team needs to navigate an increasingly complex regulatory environment without slowing your development down.
The quality, compliance, testing, and packaging solutions that protect your device programs from development through delivery.
Connect with regulatory affairs consultants, quality system specialists, and compliance experts who understand the FDA and ISO requirements your team is navigating and can help you meet them efficiently.
Find the testing tools, inspection services, and validation specialists with the capabilities to verify your device performance, safety, and reliability at every stage of development.
Explore sterilization technologies and medical device packaging solutions that protect device integrity, satisfy regulatory requirements, and support efficient production workflows.
Additional product solutions include:
The quality engineers, regulatory specialists, and compliance leaders keeping medical device programs safe, compliant, and on schedule.
Practical sessions and workshops covering the regulatory shifts, quality frameworks, and compliance strategies most relevant to quality and regulatory professionals.
Regulatory Update track sessions covering cybersecurity submissions, human factors, SaMD, and FDA pathway strategy. Built for quality and regulatory professionals navigating an ever-changing compliance environment.
Four workshops covering Right-Sized Quality Systems, Regulatory Strategy Lab, DFM, and Design Controls in Practice. The most directly relevant education at MEDevice Boston for quality and compliance teams.
Quick sessions from the regulatory consultants, testing labs, and quality solution providers on the show floor covering the latest updates and practical applications.
Two focused days in Boston connecting quality engineers, regulatory professionals, and compliance leaders with the experts and solutions that keep medical device programs on track and market-ready.