IEC 60601 & EMC Training

Delivered jointly by Lorit Consultancy and Think EMC, this training brings together expertise in IEC 60601 safety requirements and electromagnetic compatibility for medical devices.
The course is led by trainers with many years of practical experience in design, development, testing and regulatory compliance, ensuring a strong practical focus.
The IEC 60601 series defines the internationally recognised framework for ensuring the safety and performance of medical electrical equipment. It defines requirements across a broad range of hazard domains, including electrical, mechanical, thermal, and system-level risks, and establishes the basis for verification and validation activities.
Understanding IEC 60601 is key to navigating the complexity of medical device development, as it connects risk management, product design, and regulatory expectations. It also serves as a foundation for addressing collateral and particular standards, making it an integral part of bringing compliant and safe products to market.
Electromagnetic compatibility (EMC) ensures that medical devices operate safely and reliably in their intended electromagnetic environment without causing or being affected by interference. Within the medical context, this includes both emissions and immunity considerations under defined use environments, as specified in standards such as IEC 60601-1-2.
Achieving EMC compliance requires more than testing alone. It involves early design decisions, risk-based assessment, and a clear understanding of applicable regulatory frameworks and test methodologies. A structured approach to EMC helps manufacturers minimise risks, avoid costly redesigns, and ensure consistent compliance throughout the product lifecycle.
This two-day training combines IEC 60601 fundamentals with a practical introduction to electromagnetic compatibility (EMC), providing a structured view of key safety and compliance requirements for medical electrical devices.
Participants will build a solid understanding of IEC 60601, including core concepts, terminology, and the application of safety principles in product development. Through practical examples and industry insights, the course supports confident interpretation and implementation of the standard.
Building on this foundation, the training introduces EMC from both a regulatory and engineering perspective. It covers applicable standards such as IEC 60601-1-2, risk-based approaches, testing strategies, and design considerations—enabling participants to plan for compliance, avoid common pitfalls, and work effectively with test laboratories.
Duration
2 days (approx. 8 hours per day, including breaks)
Next location
Cambridge, UK
Target Audience
This training is designed for professionals involved in the development, compliance, and approval of medical electrical devices, including product safety and compliance engineers, product designers, regulatory affairs specialists, quality assurance, and production support roles.
Format
Interactive, instructor-led training combining expert presentations, practical examples, and discussion. It is delivered in-person. Group booking options are available on request.
Trainers
Alastair Walker (Lorit Consultancy), Engineering Consultant and IEC 60601 expert
James Pawson (Think EMC, Unit 3 Compliance), EMC problem solver