Executive Development Programme in Medical Device Regulatory Excellence
-- ViewingNowThe Executive Development Programme in Medical Device Regulatory Excellence is a certificate course designed to empower professionals with the necessary skills to navigate the complex regulatory landscape of the medical device industry. This programme is critical for career advancement in this field, as it provides learners with a comprehensive understanding of regulatory strategies, quality management systems, and global regulatory compliance.
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โข Introduction to Medical Device Regulatory Excellence
โข Global Regulatory Landscape for Medical Devices
โข Understanding Regulatory Pathways and Classification of Medical Devices
โข Quality Management Systems and ISO 13485 Compliance
โข Design Control and Risk Management for Medical Devices
โข Clinical Evaluation and Post-Market Surveillance
โข Labeling, Advertising, and Promotion of Medical Devices
โข Regulatory Submissions and Approvals
โข MDR, IVDR, and Post-Market Compliance
โข Global Regulatory Strategy and Harmonization Initiatives
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