Preparing for an ISO 13485 Compliance Audit A Practical Guide for Manufacturers
Автор: Riddion | Your Medical Device Regulatory Hub
Загружено: 2025-04-17
Просмотров: 52
Описание:
Preparing for an ISO 13485 audit doesn’t have to be a guessing game.
This video walks you through exactly what manufacturers need to do to get audit-ready and stay compliant.
What we cover in this guide:
Key ISO 13485 requirements auditors will focus on
Common non-conformities and how to avoid them
Documentation and records you must have in place
Tips for internal audits, CAPAs, and quality management system reviews
Discover Free Resources: www.riddionresourcehub.com
This is a must-watch for quality managers, regulatory leads, and medical device startups preparing for certification.
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