Global Certificate in ISO 13485 for MedTech

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The Global Certificate in ISO 1.

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โ€ข Introduction to ISO 13485 & Medical Devices
โ€ข Understanding ISO 13485 Requirements
โ€ข Risk Management in MedTech
โ€ข Quality Management System (QMS) Development
โ€ข Documentation Control for ISO 13485
โ€ข Training, Awareness, & Competence in MedTech
โ€ข Medical Device Design & Development Controls
โ€ข Manufacturing Process Controls & Validation
โ€ข Measurement, Analysis, & Improvement in ISO 13485
โ€ข Preparing for ISO 13485 Certification Audit

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