Release Tool:	Councils and commissions decisions
Validity:	Cancelled
Summary:	By AI The document aims to define and clarify the requirements related to the inspection and revision of the quality management system conducted by the authority on factories and medical device establishments, and to clarify the powers and rights of the inspector.

This is an earlier version ofInspection and Revision Requirements for the Quality Management System of Medical Devices and Supplies Factories and Establishments - 2025Switch to the new version

Inspection and Revision Requirements for the Quality Management System of Medical Devices and Supplies Factories and Establishments - 2025

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