• Dec 28, 2025 iec 62366 medical devices althcare, user errors can lead to serious adverse events, including incorrect diagnoses, improper treatment, or device malfunctions. IEC 62366 emphasizes proactive risk management by integrating usability considerations early By Jacqueline Murphy
• Feb 5, 2026 checklist iec 62366 strategies. Regulatory Implications and Compliance Regulatory Requirements Compliance with IEC 62366 is often a mandatory component of regulatory submissions, especially in regions like the European Union, the United States, and Canada. Regulatory bodies such as t By Camille Ward MD
