Global Certificate in Biomedical Device Regulations and AI
-- ViewingNowThe Global Certificate in Biomedical Device Regulations and AI course is a comprehensive program designed to meet the growing industry demand for professionals with expertise in biomedical device regulations and AI. This course emphasizes the importance of understanding global regulations and AI technology in the development, approval, and safety monitoring of biomedical devices.
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โข Global Biomedical Device Regulations Fundamentals: Understanding the regulatory landscape for biomedical devices on a global scale.
โข Regulatory Bodies and Compliance: An overview of key regulatory bodies and compliance requirements in major markets.
โข Quality Management Systems (QMS): The role of QMS in ensuring compliance and maintaining product quality.
โข Clinical Evaluation and Trials: Best practices for conducting clinical evaluations and trials for biomedical devices.
โข Labeling and Packaging Requirements: Compliance requirements for labeling and packaging of biomedical devices.
โข Post-Market Surveillance and Vigilance: Monitoring and reporting adverse events and maintaining device safety.
โข AI in Biomedical Devices: Overview of artificial intelligence technologies and their applications in biomedical devices.
โข Ethics and AI in Healthcare: Ethical considerations and guidelines for AI applications in healthcare.
โข AI Regulations and Compliance: Regulations and compliance requirements for AI-enabled biomedical devices.
โข AI Risk Management in Biomedical Devices: Risk management strategies for AI-enabled biomedical devices.
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