Executive Development Programme in Biocompatibility & Regulatory Affairs
-- ViewingNowThe Executive Development Programme in Biocompatibility & Regulatory Affairs is a certificate course designed to provide learners with critical insights into the rapidly evolving field of medical devices and healthcare technology. This program emphasizes the importance of biocompatibility and regulatory compliance, two essential areas in this sector.
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โข Introduction to Biocompatibility: Understanding materials and their interactions with living systems
โข Regulatory Affairs Overview: Navigating the regulatory landscape for medical devices
โข Biocompatibility Testing: Methods and standards
โข Risk Assessment and Management in Biocompatibility
โข Regulatory Affairs for Biocompatible Medical Devices
โข International Biocompatibility Standards and Regulations
โข European Medical Device Regulation (MDR) and Biocompatibility
โข US Food and Drug Administration (FDA) Regulations and Biocompatibility
โข Case Studies in Biocompatibility and Regulatory Affairs
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