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As a medical device manufacturer, ISO 13485:2016 is the most globally accepted standard of its kind. If your company wants to put competency at the heart of your operations, IMSM can tell you how this certification will improve and validate the way you work.
ISO 13485 specifies requirements for a quality management system for companies that must demonstrate their ability to supply medical devices that consistently meet customer and regulatory requirements.
In this introductory guide you will learn:
– What is ISO 13485?
– Who needs ISO 13485?
– What is involved in obtaining a certification?
IMSM can provide consultancy services to help you implement ISO 13485. For more information, download our free guide here: https://blog.imsm.com/iso-13485-digital-guide-download
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