Executive Development Programme in Biomaterials and Regulatory Compliance
-- ViewingNowThe Executive Development Programme in Biomaterials and Regulatory Compliance is a certificate course designed to equip learners with the essential skills needed for career advancement in the biomaterials industry. This course is crucial in a time when biomaterials play an increasingly important role in healthcare, from medical devices to drug delivery systems.
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โข Introduction to Biomaterials: Definition, history, and classification of biomaterials, properties, and biocompatibility
โข Biomaterials in Medical Devices: Applications, design, and performance of biomaterials in various medical devices
โข Biomaterials in Tissue Engineering: Scaffolds, cells, and signaling molecules, tissue engineering strategies
โข Regulatory Landscape for Biomaterials: Overview of regulatory bodies, regulations, and guidelines for biomaterials and medical devices
โข Risk Management in Biomaterials: Hazard identification, risk assessment, and mitigation strategies
โข Clinical Trials and Post-Market Surveillance: Study design, data collection, and analysis, post-market surveillance and reporting
โข Quality Management Systems: ISO 13485, quality management principles, and best practices
โข Biomaterials Testing and Characterization: Test methods, standards, and techniques for biomaterials characterization
โข Ethical Considerations in Biomaterials Research: Ethical principles, research integrity, and patient safety
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