Certificate in ISO 13485 for Regulatory Affairs
-- ViewingNowThe Certificate in ISO 13485 for Regulatory Affairs is a vital course for professionals seeking to excel in the medical device industry. This certification program focuses on the international standard for medical device quality management systems, ISO 13485.
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โข Introduction to ISO 13485 & Regulatory Affairs
โข Understanding Medical Device Regulations
โข Quality Management System (QMS) Requirements
โข Implementing ISO 13485: Key Components
โข Risk Management in ISO 13485
โข Documentation Control for ISO 13485
โข Internal Audits and Management Review
โข CAPA Management in ISO 13485
โข Preparing for ISO 13485 Certification Audit
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