IMQ supports medical device manufacturers with product and management system certification and audit and inspection services.
With regard to product certification, IMQ has obtained all the necessary notifications and accreditations to certify and audit the conformity of medical devices, both electrical and non-electrical. As well as certifying products for the European market (IMQ is a notified body for carrying out conformity assessment procedures on medical devices pursuant to Regulation (EU) No. 2017/745 that repeals Directive 93/42 /EEC and Directive 90/385/EEC.
IMQ is also accredited to certify management systems in accordance with ISO standards.