Executive Development Programme in IVD Regulatory Affairs Management
-- ViewingNowThe Executive Development Programme in IVD Regulatory Affairs Management certificate course is a comprehensive program designed to meet the growing industry demand for experts in the field of in vitro diagnostic (IVD) devices. This course emphasizes the importance of regulatory compliance and management in the IVD industry, providing learners with essential skills and knowledge to advance their careers.
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โข IVD Regulatory Affairs Management Overview
โข Understanding IVD Regulations and Standards
โข Global IVD Regulatory Landscape
โข Quality Management System for IVDs
โข Clinical Evidence and Evaluation for IVDs
โข IVD Regulatory Submissions and Approvals
โข Post-Market Surveillance and Vigilance in IVDs
โข IVD Labeling, Advertising, and Promotion
โข Risk Management in IVD Regulatory Affairs
โข Trends and Future Developments in IVD Regulatory Affairs
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- BasicUnderstandingSubject
- ProficiencyEnglish
- ComputerInternetAccess
- BasicComputerSkills
- DedicationCompleteCourse
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- NotAccreditedRecognized
- NotRegulatedAuthorized
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- ThreeFourHoursPerWeek
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- TwoThreeHoursPerWeek
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