Certificate in Medical Device Regulations and Ethics

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The Certificate in Medical Device Regulations and Ethics course is a comprehensive program designed to provide learners with essential knowledge in medical device regulations, ethics, and quality assurance. This course is vital for professionals working in or seeking to enter the medical device industry, where understanding compliance is critical for career advancement.

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The course covers global regulatory frameworks, European Union Medical Device Regulation (MDR), U.S. Food and Drug Administration (FDA) requirements, and ethics in medical device development and clinical trials. Learners will gain skills in risk management, quality management systems, and post-market surveillance, making them valuable assets in the medical device sector. Upon completion, learners will be equipped with the necessary skills to navigate the complex regulatory landscape and ensure compliance, ethical conduct, and overall success in medical device innovation. High industry demand and an increasing focus on safety and compliance make this course an excellent opportunity for career development and growth in the medical device field.

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โ€ข Introduction to Medical Device Regulations
โ€ข History and Evolution of Medical Device Regulations
โ€ข Global Medical Device Regulatory Bodies
โ€ข Medical Device Classification and Regulation
โ€ข Regulatory Pathways for Medical Devices
โ€ข Quality System Regulation and Good Manufacturing Practices
โ€ข Clinical Evaluation and Clinical Data for Medical Devices
โ€ข Medical Device Labeling, Instructions for Use, and Promotion
โ€ข Post-Market Surveillance and Vigilance
โ€ข Ethical Considerations in Medical Device Research and Development

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็คบไพ‹่ฏไนฆ่ƒŒๆ™ฏ
CERTIFICATE IN MEDICAL DEVICE REGULATIONS AND ETHICS
ๆŽˆไบˆ็ป™
ๅญฆไน ่€…ๅง“ๅ
ๅทฒๅฎŒๆˆ่ฏพ็จ‹็š„ไบบ
London School of International Business (LSIB)
ๆŽˆไบˆๆ—ฅๆœŸ
05 May 2025
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