Executive Development Programme in IVD Regulatory Affairs Management Strategies
-- ViewingNowThe Executive Development Programme in IVD Regulatory Affairs Management Strategies certificate course is a comprehensive program designed to equip learners with critical skills in managing regulatory affairs for In Vitro Diagnostic (IVD) devices. This course highlights the importance of regulatory compliance in the IVD industry and the role of effective management strategies in driving business success.
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โข IVD Regulatory Affairs Management
โข Understanding the IVD Regulatory Landscape
โข Global IVD Regulations (e.g., EU IVDR, US MDR, China NMPA)
โข Compliance Strategies for IVD Manufacturers
โข Quality Management Systems in IVD Regulatory Affairs
โข Clinical Evidence and Data Requirements for IVDs
โข Post-Market Surveillance and Vigilance in IVD Regulatory Affairs
โข Risk Management in IVD Regulatory Affairs
โข IVD Labeling, Packaging, and Distribution
โข Strategic Planning for IVD Regulatory Affairs
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