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EN ISO 13485 - for which customers?
This standard is aimed at manufacturers of medical devices who must comply with international, Europ
Mar 10, 2022
# ISO 13485
# MDSAP- Medical Device Single Audit Program
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MED unannounced audits
Important information about your admission procedure
Mar 10, 2022
# CE marking
# Health care certifications
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What does a quality management representative do?
In everyday corporate life, those responsible for a quality management system are often referred to
Mar 10, 2022
# Quality management requirements
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Interested parties easily explained
Interested parties are an inescapable part of the "context" of any business. No matter what size or
Mar 09, 2022
# Quality management requirements
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Change of certifier and/or notified body
You want to change to a different certifier and/or the notified body, but how? Our step-by-step appr
Mar 09, 2022
# Health care certifications
# CE marking
# ISO 13485
# Primary packaging materials for medicinal products
# MDSAP- Medical Device Single Audit Program
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What does compliance mean?
 The English word compliance has Latin roots. In the context of business law, it means something li
Mar 09, 2022
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