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Principles of In Vitro Diagnostic (IVD) Medical Devices Classification

Origin/Publisher:

GHTF

Document Type:
Guideline
Content:
This document has been developed to encourage and support global convergence of regulatory systems. It is intended for use by Regulatory Authorities, Conformity Assessment Bodies and industry, and will provide benefits in establishing, in a consistent way, an economic and effective approach to the control of medical devices in the interest of public health.

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