ISO 13485 training equips professionals in the medical device industry with the knowledge to implement, manage, and audit a Quality Management System (QMS) that meets regulatory and customer requirements. Covering key topics like risk management, documentation control, and regulatory compliance, this training ensures adherence to international standards for medical device safety and effectiveness. Designed for quality managers, auditors, and regulatory professionals.
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https://iasiso-asia.com/LK/iso....-13485-lead-auditor-
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