Executive Development Programme in MedTech Regulatory Updates
-- ViewingNowThe Executive Development Programme in MedTech Regulatory Updates is a certificate course designed to provide learners with the latest regulatory developments in the medical technology industry. This programme emphasizes the importance of staying updated with regulatory changes to ensure compliance, minimize risks, and drive innovation in MedTech.
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โข MedTech Regulatory Updates Overview
โข Global MedTech Regulatory Landscape
โข European Medical Device Regulation (MDR) & In Vitro Diagnostic Regulation (IVDR)
โข US Food and Drug Administration (FDA) Regulations for Medical Devices
โข Regulatory Requirements for Software as a Medical Device (SaMD)
โข Clinical Evaluation and Post-Market Surveillance
โข Quality Management Systems for MedTech Companies
โข MedTech Regulatory Submissions & Documentation
โข Global Harmonization & International MedTech Regulations
โข Emerging Trends in MedTech Regulatory Affairs
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EntryRequirements
- BasicUnderstandingSubject
- ProficiencyEnglish
- ComputerInternetAccess
- BasicComputerSkills
- DedicationCompleteCourse
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- NotAccreditedRecognized
- NotRegulatedAuthorized
- ComplementaryFormalQualifications
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- ThreeFourHoursPerWeek
- EarlyCertificateDelivery
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- TwoThreeHoursPerWeek
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