Industry & Medical

Reliability, compliance and product performance for critical markets

The Emitech Group supports manufacturers of industrial and medical equipment in the validation, conformity and reliability of their products.

Whether for industrial machinery, embedded systems or medical devices, our expertise covers the entire cycle: design, testing, qualification and marketing.

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Industrial and medical sectors
Industry & consumer sector

Industry

Machine tools, production equipment, electrical cabinets, handling systems: we can help you with your EMC, electrical safety, mechanical and environmental testing needs to guarantee the robustness and availability of your products in demanding industrial environments.

Medical sector

Medical

Medical devices (MDs), laboratory equipment, paramedical equipment: regulations are strict, reliability is critical. We can help you get your products on the market in accordance with Regulation (EU) 2017/745, anywhere in the world.

Our cross-disciplinary services

For each of these sectors, the Emitech Group offers:

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Why choose the Emitech Group?

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Needs

Discover a selection of additional resources that explore topics related to this page including regulatory contexts, technical articles, and specific areas of expertise. These materials provide further insight to help you better understand the key challenges and available solutions.

Directive RED 2014/53/EU - CE marking

Guarantee the compliance of your radio equipment with the RED Directive 2014/53/EU: testing, cybersecurity, CE marking and certification with Emitech Certification, a Notified Body.
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EMC Directive 2024/30/EU - CE marking

Comply with the requirements of the EMC Directive 2014/30/EU: EMC (electromagnetic compatibility) tests, technical file, EU declaration of conformity, CE marking and expert support.
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Machinery Directive - CE marking

We can help you demonstrate compliance with the Machinery Directive 2006/42/EC and Machinery Regulation 2023/1230, which ensures the safety of machinery and equipment as part of the CE marking.
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North American market - FCC/ISED and NRTL Safety

Access the North American market with FCC/ISED (EMC and radio frequency) and UL, ETL, CSA... certifications.
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CB Scheme / CB Scheme

The CB Scheme enables manufacturers of electrical products to benefit from mutual recognition of tests, making it easier to obtain national certification.
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CE marking for medical devices and IVDDs

We can help you demonstrate compliance with the MDR 2017/745 regulation for Medical Devices (and the DM DIV 2017/746 regulation for your In Vitro Diagnostic Medical Devices - IVDR).
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CE marking

The CE marking is a sign certifying that a product complies with the essential safety, health and environmental protection requirements laid down by the European Union, and allowing it to circulate freely in the European Economic Area.
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Comprehensive support tailored to your needs

Are you developing a medical device, industrial equipment or embedded system?

Contact our experts to define a comprehensive qualification plan and ensure the compliance, reliability and performance of your products before they are launched on the market.

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