Executive Development Programme in MedTech Regulatory Landscapes
-- ViewingNowThe Executive Development Programme in MedTech Regulatory Landscapes is a vital certificate course designed to meet the growing demand for professionals with a deep understanding of the complex regulatory frameworks in the MedTech industry. This programme equips learners with essential skills to navigate the intricate web of regulations and standards, ensuring compliance and driving innovation.
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โข MedTech Regulatory Landscapes Overview
โข Global Medical Device Regulations
โข US FDA Regulations for Medical Devices
โข European Medical Device Regulation (MDR) & In Vitro Diagnostic Regulation (IVDR)
โข Regulatory Affairs for MedTech: Roles and Responsibilities
โข Clinical Evaluation and Clinical Trials in MedTech
โข Quality Management Systems in MedTech: ISO 13485
โข Post-Market Surveillance and Vigilance in MedTech
โข MedTech Regulatory Submissions and Documentation
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