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ISO 13485:2016
ISO 13485:2016 Is That The Commonplace For A Top Quality Management System (“QMS”) For The Planning And Manufacture Of Medical Devices. Certification To The Quality Needs Associate Degree Organization's Quality Management System To Pass A Third-Party Medical Device Single Program Know More
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About
ISO 13485:2016
ISO 13485:2016 is that the commonplace for a top
quality Management System (“QMS”) for
the planning and manufacture of Medical Devices. Certification to the quality needs
associate degree organization's quality management system to
pass a third-party Medical Device Single program, or “MDSAP” Audit. For the foremost part:
ISO 13485 = ISO 9001 + further Medical Device necessities.
While ISO 13485:2016 remains a complete document, it aligns with ISO 9001:2008. (Yes, 2008,
not 2015.) this can be as a result of
it doesn't follow the high-level structure (Annex L) of the most recent version of ISO 9001
(which is 9001:2015). additionally, the documentation
and safety necessities square measure a lot of larger underneath ISO 13485:2016, whereas ISO
9001:2015 puts target client satisfaction and continuous improvement.
This international commonplace is obligatory in some countries, and within the U.S. the
authority has planned a rule which might harmonize U.S. authority twenty one CFR 820 with
ISO 13485:2016, creating ISO 13485 the FDA's obligatory QMS for Medical Devices (the rule is
predicted to be discharged in 2019).
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Steps For ISO 13485:2016
BENEFITS
Benefits of iso 13485:2016
- iso 13485 implementation ensures you continuous improvement
- it assist in cutting costs, increasing efficiency and monitoring performance
- iso 13485 serves as a regulatory or legal requirements in many countries
- iso 13485 firmly ensure the use of best practices throughout all steps of a medical device's life cycle
- it enables you to offer safer and more qualitative products and services to customer
