Masterclass Certificate in Biomedical Tech: Regulatory Updates
-- ViewingNowThe Masterclass Certificate in Biomedical Tech: Regulatory Updates is a comprehensive course designed to provide learners with the latest regulatory knowledge and skills required in the biomedical technology industry. This course is crucial for professionals seeking to stay updated with changing regulations and compliance norms, ensuring the safety and efficacy of biomedical products.
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โข Regulatory Affairs in Biomedical Technology
โข Understanding FDA Regulations for Biomedical Devices
โข European Medical Device Regulation (MDR) and In Vitro Diagnostic Device Regulation (IVDR)
โข Global Harmonization Task Force (GHTF) and International Medical Device Regulators Forum (IMDRF)
โข Quality System Regulation (QSR) and Good Manufacturing Practices (GMP)
โข Post-Market Surveillance and Adverse Event Reporting
โข Clinical Trials Regulation and Compliance
โข Biocompatibility and Sterilization Requirements
โข Risk Management and Usability Engineering in Biomedical Technology
โข Updates and Trends in Biomedical Technology Regulations
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