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Health care certifications



Health care certifications

ISO 9001, ISO 13485, MDSAP, ISO 15378

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Product
MDSAP Medical Device Single Audit Program
Medical devices in the international environment
Product
Regulation MDR (EU) 2017/745
CE marking for medical devices
Product
ISO 13485
Quality management systems for medical devices
Blog
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CE marking: Notes on handling unannounced audits

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Change of certifier and/or notified body

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MED unannounced audits

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medizinprodukte-zertifizierungsdokumente

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

What to consider when submitting your technical documentation

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DQS MED presentation slides

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Who we are - DQS Medizinprodukte GmbH

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Topics that may interest you
# Primary packaging materials for medicinal products # ISO 13485 # CE marking # MDSAP- Medical Device Single Audit Program

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