Notified Body certification and audit services for medical devices under EU MDR 2017/745. DQS provides independent assessment, compliance evaluation, and accreditation for manufacturers entering European markets, supported by four decades of expertise across 60+ countries.
Manufactured by
DQS Medizinprodukte GmbH
Frankfurt, Germany
With our audits, we create more security and higher process quality across all industries. Our work ranges from the certification of management systems to audits relating to medical products, information security and sustainability. Are you looking for high-quality professional information on the subject of assessment and certification? Then you've come to the right place. On the following pages, we offer you a broad portfolio of topics that are covered in depth by our experts. Get standards knowledge here that will broaden your perspectives and sharpen your eye for detail. Find out more with our free range of whitepapers and webinars - live or recorded. Do some research in our online specialist magazine or take part in one of our training courses. We are also happy to come to your company with our in-house training courses.
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BEO MedConsulting Berlin GmbH
Germany · 1 relevant product
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MARGOMED S.A.
Poland · 1 relevant product
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BEO MedConsulting Berlin GmbH · Germany
Regulatory consulting and quality management system implementation for medical device manufacturers. Supports EU-MDR 2017/745 compliance assessments, conformity documentation, and QMS establishment. Includes regulatory documentation, expert evaluations, and audit coordination to ensure product safety and market authorization.
IMQ Certification (Shanghai) Co., Ltd. · China
EU MDR Certification service for medical devices ensures compliance with European Medical Device Regulation requirements. This certification validates product safety, performance, and quality management systems for market authorization in EU member states.
MARGOMED S.A. · Poland
Quality assurance and regulatory compliance support for medical device manufacturers. Ensures products meet MDR 2017/745 and EN ISO 13485:2016 standards.
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