Intertek — Usability Engineering for Medical Devices: IEC 62366
Summary
Intertek’s resources on usability engineering and human factors for medical devices, aligned with IEC 62366 and MDR Annex I general safety and performance requirements. Covers usability engineering files, formative and summative evaluations, and risk-based approaches to user interface design.
Document Details
Document IDINTERTEK-USABILITY
TypeWhite Paper
AuthorityIntertek (NB 0413)
Publication Date2023-10-01