Professional Certificate in Medical Device Regulatory Affairs Best Practices
-- ViewingNowThe Professional Certificate in Medical Device Regulatory Affairs Best Practices course is a comprehensive program designed to equip learners with the essential skills needed to thrive in the medical device industry. This course highlights the importance of regulatory affairs by teaching best practices, industry standards, and compliance requirements.
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⢠Medical Device Regulations Overview
⢠Global Regulatory Landscape for Medical Devices
⢠Quality Management Systems in Medical Device Regulatory Affairs
⢠Regulatory Strategy and Product Lifecycle Management
⢠Clinical Data and Regulatory Submissions
⢠Medical Device Classification and Risk Management
⢠Labeling, Packaging, and Sterilization Requirements
⢠Post-Market Surveillance, Vigilance, and Complaint Handling
⢠International Medical Device Regulations (e.g., EU MDR, MDSAP, FDA)
⢠Regulatory Affairs Best Practices and Compliance
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