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Designing for Compliance to IEC 60601-1 3rd Edition - Live Virtual Classroom - Session 1: Medical Equipment and Systems: Role of the IEC around the Globe; 3rd Edition Regulatory update; Structure and Scope of 60601-1; Equipment Classifications


Presented by experienced UL engineers knowledgeable in evaluating products for certification to U.S. and international standards for medical equipment, this live virtual workshop will help you gain an understanding of the following topics in our curriculum related to Medical Equipment and Systems – Designing for Compliance to 60601-1:2005.

This session is one of eight virtual sessions on the subject of “Designing for Compliance to IEC 60601-1 3rd Edition” that are offered either individually or as a bundled offering of all eight topics. If you wish to take the complete bundle of topics related to 60601-1 3rd Edition, click here for a full description and bundled pricing.


Workshop Topics:

  • Role of the IEC Around the Globe
  • Structure of IEC 60601-1 and ES 60601-1
  • General Philosophy of IEC 60601-1
  • Equipment Classifications and Scope of Standard


  • Recognize the full scope of IEC 60601-1, including the current deviations:
  • US (ANSI/AAMI ES 60601-1)
  • European (EN 60601-1) deviations.
  • Determine the applicable medical equipment requirements to design products for compliance.
  • Interpret world certification schemes and agreements affecting medical equipment.

Target Audience

  • Product safety engineers
  • Compliance engineers
  • Product designers
  • Regulatory approval staff
  • Production support engineers
  • Quality assurance staff Technical marketing professionals
Click here for terms and conditions...


Time Requirement


Instructor-Led 2 hours 30 minutes $250.00

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