Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
EU RoHS 2 Directive 2011/65/EU
Through training, testing and certification, Intertek’s team of medical product compliance experts can help you define and develop your product’s technical file content and process controls to ensure your device meets the requirements of the RoHS 2 Directive.
In effect since July 21, 2011, RoHS 2 identifies six regulated substances - lead, mercury, cadmium, hexavalent chromium, polybrominated biphenyls, and polybrominated diphenyl ether - restricted in manufacturing certain electrical and electronic equipment sold in the EU. The scope of the Directive extends to all electrical and electronic equipment within 11 broad categories, including:
Partner with Intertek to learn more about making strategic decisions for medical product compliance.
Intertek does not provide consulting services for management systems certification. Any consulting activities provided by Intertek are separate and independent from certification activities.
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