-
HTMA Collaborative: UCONN Clinical Engineer Student Showcase (Mar 2026)
Join the New England Society of Clinical Engineering (NESCE) and the University of Connecticut’s renowned Clinical Engineering Masters Program for…
-
AAMI 2026 Voting: Board Directors, Chairs, and Re-election
The AAMI Nominating Committee has put forth a slate of new leaders to serve on the AAMI Board of Directors. Members, your vote matters! Participating members should expect an email in to their registered account.
-
The Quality Management System Regulation (QMSR) (Mar26)
This 4.5 day course is the culmination of years of consensus development on the part of a respected group of quality system experts from leading device manufacturers, the FDA, industry consultants, and members of International Organization for Standardization (ISO) standards development teams.
-
Who is Speaking at AAMI eXchange 2026?
Get to know the individuals defining leadership, improving world device accessibility, and impacting your HTM department on the ground floor.
-
Practical HTM Career & Leadership Development Program with Danielle McGeary
Develop the skills, confidence, and strategic mindset to advance your HTM career within your organization—and elevate the value your department…
-
Federal Regulators Outline AI Priorities at HIMSS/AMDIS Physicians’ Forum
Federal health leaders at the HIMSS/AMDIS Physicians’ Forum discussed the administration’s priorities for artificial intelligence, highlighting regulatory coordination, emerging oversight models, and AI’s potential to address workforce shortages and improve…
-
Event Host Open To: Members and Non-members Event Schedule by Time Zone: Pacific: 10 AM to 11 AM | Mountain: 11 AM to 12 PM | Central: 12 PM to…
-
From AI Hype to Healing: Leading Clinician Shares Hope for an AI Renaissance
Can AI return clinicians to the bedside? At HIMSS 2026, Jesse Ehrenfeld, MD, envisions AI handling data overload while doctors reclaim the art of medicine—but only if governance, trust, and “techquity” guide its deployment.
-
Navigating 510k & DeNovo Requirements (Nov26)
This 4-day course will navigate the 510(K) clearance process and De Novo classifications requests for United States (U.S.) and global Medical Device…
-
Production & Quality System Software (Nov26)
This course is designed to understand what is and what is not production and quality system software that is required to be validated by FDA and ISO…
-
-
Design Control Requirements – Integrating the Quality System Regulation (Dec26)
This intensive 3 – day course provides complete coverage of design control requirements for FDA Quality System Regulation, ANSI/AAMI/ISO…
-
Process Validation Requirements & Industry Practices (Dec26)
This 3-day course provides attendees with practical tools and techniques for process validation requirements for FDA’s Quality System Regulation…
-
Human Factors for Medical Devices (Dec26)
Medical device manufacturers with robust human factors processes are leading the market, proving to have better clinical outcomes and better quality….
-
Integrating Risk Management into the Product Life Cycle (Oct26)
Join us a develop a comprehensive understanding of risk management concepts used throughout the quality management system to consistently meet FDA 21…
- Load More








