Certificate in ISO 13485 Documentation
-- ViewingNowThe Certificate in ISO 13485 Documentation course is a professional development program that focuses on the creation and management of quality management systems in the medical device industry. This course is essential for those looking to advance their careers in this field, as it provides learners with the necessary skills to ensure compliance with regulatory requirements and industry best practices.
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⢠Introduction to ISO 13485
⢠Understanding ISO 13485 Documentation Requirements
⢠Developing a Quality Manual for ISO 13485
⢠Creating Procedures and Work Instructions
⢠Design and Development Controls for Medical Devices
⢠Document Control and Record Management
⢠Internal Audit and Management Review
⢠Corrective and Preventive Action Process
⢠Training and Competence for ISO 13485
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