DQS Medizinprodukte GmbH offers various services in the field of approval of medical devices and certification of management systems in healthcare. With our competence, experience and range of services, we can give you a real competitive edge. The value of and trust in our certificates are essential for us and our customers. We stand by this with our commitment to impartiality and independence in the performance of our certification activities.

CE marking

MDR (EU) 2017 / 745

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Price list of standard fees for the MDR

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CE marking: Notes on handling unannounced audits

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Flatten-the-Curve? From 2023, the big wave of MDR certifications will be rolling in for notified bodies

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Change of certifier and/or notified body

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MED unannounced audits

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medizinprodukte-zertifizierungsdokumente
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When is software a medical device under the MDR?

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What to do with so-called "material" medical devices under the MDR?

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Great Britain's exit from the EU and the consequences for the medical device market

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medizinprodukte-zertifizierungsdokumente
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What to consider when submitting your technical documentation

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Richtlinie 93/42/EWG für Medizinprodukte
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DQS Medizinprodukte GmbH, Member of DQS Group

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What to do with reusable surgical instruments of class "Ir" under the MDR?

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DQS MED presentation slides

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Who we are - DQS Medizinprodukte GmbH

Primary packaging materials for medicinal products

ISO 15378

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Change of certifier and/or notified body

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DQS MED presentation slides

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Who we are - DQS Medizinprodukte GmbH