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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⢠MedTech Regulatory Updates Overview
⢠Global MedTech Regulatory Landscape
⢠European Medical Device Regulation (MDR) & In Vitro Diagnostic Regulation (IVDR)
⢠US Food and Drug Administration (FDA) Regulations for Medical Devices
⢠Regulatory Requirements for Software as a Medical Device (SaMD)
⢠Clinical Evaluation and Post-Market Surveillance
⢠Quality Management Systems for MedTech Companies
⢠MedTech Regulatory Submissions & Documentation
⢠Global Harmonization & International MedTech Regulations
⢠Emerging Trends in MedTech Regulatory Affairs
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