Organizations across the world trust Nemko to assess their products, systems, and devices for conformity with relevant medical device standards and regulations according to their location.
For more than 85 years, Nemko has ensured that our customers understand and comply with their country’s standards and regulations through the testing, documentation, and successful approval process. We provide services such as pre-compliance, international approval, product and system certifications, and product testing.
Nemko offers local presence powerfully combined with global knowledge.
Helping You Stay One Step Ahead
Your local Nemko team of experts will handle projects through every step of the process and follow up on delivery, keeping your team apprised of any regulatory changes that may occur in the future.
Nemko test reports and certificates are internationally recognized and accepted for national approval processes across the globe.
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Before a test can begin, there is a preparation and planning period to establish the testing schedule, which will in turn make sure your tests are performed as efficiently as possible.
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Medical devices are among the most highly regulated products found in the market today. Make sure your product complies with these standards to ensure the highest level of safety at all times.
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During the testing process, there can be issues that come up and stall the timeline of the project. Nemko offers complete project management expertise to avoid any unnecessary delays.
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Nemko offers comprehensive global EMC testing and certification services within regulatory requirements for a wide range of electro-medical devices.
Read MoreCollaborative compliance
Compliance requirements are easier to meet when they’re part of the development process, not an afterthought. Nemko helps product teams identify potential issues earlier to reduce rework and simplify the path to approval.





