SATELLITE™ empowers medical device manufacturers to add more speed, efficiency, and cost-savings into their compliance program
Intertek’s SATELLITE™ Client Test Program revolutionizes compliance for medical device manufacturers, giving you the ability to perform testing in your own facilities while maintaining adherence to critical standards like IEC 60601-1, IEC 60601-1-2, and IEC 61010. Whether you’re developing medical imaging equipment, implantable devices, or Home Healthcare technologies, SATELLITE provides a flexible framework that accelerates testing and certification while ensuring global compliance.
By integrating compliance into your product development lifecycle, the SATELLITE program reduces delays and eliminates reliance on third-party lab availability. With customizable testing protocols, it addresses the complexities of modern medical devices, including high component counts and supply chain challenges. This flexibility ensures your devices meet regulatory requirements such as FDA approval and CE marking while expediting global market entry.
SATELLITE’s scalable solutions allow you to retain control over the testing process, from partial oversight to full autonomy. Manufacturers gain the agility needed to adapt to evolving standards and regulatory landscapes, ensuring safety and performance while staying competitive. Take control of your compliance with Intertek’s SATELLITE program and bring innovative medical devices to market faster and with greater confidence.
Discover how Intertek's SATELLITE™ Client Test Program can revolutionize your medical device testing and certification with unmatched control, cost savings, and speed to market.
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Conduct product testing in your own labs and on your own schedule while obtaining our market-leading Certifications with our SATELLITE™ Client Test Program
Knowledge Center
Download the latest information from our medical device compliance experts
Creation of IEC 60601-1 4th Edition
IEC 60601-1-2 Ed. 4.1 Overview of Requirements
Medical OEM Wireless Coexistence Testing
Artificial Intelligence (AI) and Machine Learning (ML) in Medical Devices
Biocompatibility Risk Assessment and Evaluation Plans
For more expert papers, recordings, and presentations, visit our Medical Resources hub.
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** The Intertek legal entities that provide medical device management system certification services (including ISO 13485 and MDSAP) and Notified Body services (MDR 2017/745 and MDD 93/42/EEC) do not provide any consulting services. Clients who have used other Intertek legal entities’ consulting services are not eligible to receive management system certification services or Notified Body services from Intertek.