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ITENA Clinical is committed to implement its quality system according to the requirements of  ISO 13485: 2012, the Medical Devices Directive 93/42 / EEC, FDA regulation and Health Canada to offer products which meet standards and regulatory requirements.

2012 was the opportunity for ITENA Clinical to open new perspectives by complying with the American and Canadian regulations to open new business horizons.

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> Download Certificate FR05/66739 Directive 93/42/EEC