DQS Academy provides specialized training and certification programs for medical device manufacturers and healthcare organizations. Courses cover EU Medical Device Regulation (MDR) compliance, quality management systems (ISO 13485), and notified body assessment requirements. Delivered by industry ex...
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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SigmaTech Nordic · Denmark
QA training program supporting medical device companies in achieving CE marking compliance and ISO 13485 certification. Covers regulatory requirements, quality management systems, and documentation standards for diagnostic and therapeutic devices across European markets.
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ISO 13485 Lead Auditor training course for medical device professionals. Equips quality and regulatory personnel with accredited credentials for implementing and auditing Quality Management Systems in medical device manufacturing. Includes theoretical knowledge and practical competency assessment aligned with international standards.
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Training and certification services for medical device manufacturers covering global regulatory standards, quality management systems (ISO 13485), and conformity assessment. Enables organizations to achieve compliance with international medical device regulations and obtain necessary notified body approvals for market placement.
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