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Quality Management System – Medical Devices – Guidance on the Control of Products and Services Obtained from Suppliers
Origin/Publisher:
GHTF
Document Type:
Guideline
Content:
This guidance document is intended for medical device manufacturers and it is expected that the
reader is familiar with regulatory quality management system requirements within the medical
devices sector. This guidance document may also be useful to regulatory authorities and
suppliers. This guidance document is intended for educational purposes and it is not intended to
be used to assess or audit compliance with regulatory requirements.
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