[Webinar Series on Medical Device Safety Standards from the Basics 2025] Session 2: Electromagnetic Interference/EMC Testing for Medical Electrical Equipment (IEC 60601-1-2)

We will explain an overview of IEC 60601-1-2, including electromagnetic interference testing and changes from the 4th edition to the 4.1 edition.

[Webinar Series on Medical Device Safety Standards from the Basics 2025] Session 2: Electromagnetic Interference/EMC Testing of Medical Electrical Equipment (IEC 60601-1-2) March 25, 2025 | Free | Online Technical standards for medical devices are complex and varied, including the IEC 60601-1 series and individual standards from the IEC 60601-2 series. In recent years, revisions to EMC standards have been made, and the transition period to the JIS standard JIS T 0601-1-2:2023 is approaching in mid-February 2026. In this webinar, as part of the introductory series on medical device safety standards for 2025, we will provide an overview of IEC 60601-1-2, explain electromagnetic interference testing, and discuss changes from the 4th edition to the 4.1 edition. Additionally, we will introduce some testing methods for basic standards that were requested in last year's survey. For more details and to register, please follow the link below.

• Other Testing Contract

Manufacturers need to demonstrate compliance with regulations regarding safety and performance requirements to ensure product safety and market entry.

Medical device manufacturers need to demonstrate compliance with numerous regulations regarding electromagnetic compatibility (EMC), wireless performance, radio frequency (RF) exposure, and other safety and performance requirements to ensure product safety and market entry. UL Solutions provides comprehensive support and guidance from design concept to product completion, helping to avoid potential issues and reduce time to market.

• EMC Testing

One-stop service for on-site measurements, requests, and compliance with radio laws in various countries.

UL Solutions supports a wide range of products, from IT/AV equipment to wireless devices, automotive/construction machinery, and medical devices. Our specialists, based on proven results and experience, provide meticulous support not only for testing but also for certification acquisition. 【Features】 - Wide range of products supported, from IT/AV equipment to wireless devices, automotive/construction machinery, and medical devices - Support for both testing and certification acquisition - Testing laboratory operates based on the ISO/IEC 17025 standard - Support for overseas expansion 【Benefits of Using UL Solutions】 The UL Solutions EMC testing laboratory is accredited by the U.S. NVLAP, the Japan Accreditation Board (JAB), and A2LA, based on the operational standard ISO/IEC 17025. We meet various requests for a wide range of products, from IT/AV equipment to wireless devices, automotive/construction machinery, and medical devices, including compliance with general EMC standards and radio wave regulations in various countries. Specialists with iNARTE (EMC technical qualification) provide meticulous support tailored to each customer's needs. *For more details, please refer to the PDF document or feel free to contact us.

• EMC Testing

Providing solutions for the global market.

UL Solutions provides evaluation testing and certification in accordance with product safety standards and EMC standards, biocompatibility testing, reprocessing validation, packaging validation, and ISO 13485 audit registration services to manufacturers of medical devices, in vitro diagnostic medical devices, laboratory equipment, and testing/measurement equipment.

• Other contract services

Compliance with IEC 60601, IEC 61010, and various individual standards.

Our company is one of the NRTLs (Nationally Recognized Testing Laboratories) recognized by the U.S. OSHA, and we are also a CB accredited testing laboratory certified by IECEE in the fields of medical electrical equipment and in vitro diagnostic medical devices. Additionally, we are an ILAC accredited testing laboratory registered with the International Accreditation Service, Inc. (USA). The evaluation reports and certifications we provide can be used for medical device and in vitro diagnostic medical device regulatory submissions in various countries.

• Contract Inspection

In this webinar by SPT Labtech and Alithea Genomics, we will introduce practical methods to eliminate bottlenecks in library preparation, from single-cell RNA-seq to bulk RNA-seq. - Streamlining rare cell workflows: By combining FLASH-seq and firefly, we can complete full-length scRNA-seq library preparation from low-input or FACS-sorted samples in one day. - Scaling up bulk RNA-seq: Achieve high-throughput screening compatible with 96/384 well plates using extraction-free, plate-based solutions like Total DRUG-seq. - Accelerating the process from sample to data: We will provide practical tips for reducing manual work and smoothly integrating automation. - Case studies: We will demonstrate the effectiveness through case studies and real data in various applications of RNA-seq.

Join our expert webinar to discover how SPT Labtech's mosquito liquid handler is transforming the approach to assay miniaturization. - Smartly scaling up workflows at the nanoliter scale: Learn how to optimize existing genomics, screening, and chemistry protocols for ultra-low volumes, and the new possibilities that arise from this. - Considering value beyond cost reduction: Miniaturization enables innovative applications such as single-cell omics, workflows for direct processing from cells, and optimization of parallel reactions. Real case studies: We will present examples of academic and industrial labs that have successfully scaled up their research using mosquito.

Our company will be exhibiting equipment at the "Mediseo Medical Fair 2025 in Tokai." We sincerely look forward to your visit.

As you advance the utilization of AI, you may face challenges such as "while certain results are achieved in validation, they do not translate into operational use," "the model has been created, but it cannot be implemented into measures, making ROI difficult to explain," and "collecting and preprocessing the data for utilization takes time." This presentation will explain a method to streamline data preparation with no-code solutions, generate key features that are essential for AI accuracy, train them using the latest algorithms, and automate the implementation up to actual marketing measures.

Nihon Jet-On Co., Ltd. will be exhibiting at the "Surface Modification Exhibition 2025" held at Tokyo Big Sight. This exhibition is a comprehensive showcase of surface treatment technologies, introducing various techniques that achieve improved wear resistance and extended lifespan through processes such as heat treatment and plating, thereby enhancing added value and functionality. We sincerely look forward to your visit.