Executive Development Programme in Medical Device Regulatory Risk Management

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The Executive Development Programme in Medical Device Regulatory Risk Management is a certificate course designed to empower professionals with the necessary skills to navigate the complex regulatory landscape of the medical device industry. This programme is crucial in today's context due to the increasing demand for experts who can manage regulatory risks and ensure compliance with intricate medical device regulations.

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ใ“ใฎใ‚ณใƒผใ‚นใซใคใ„ใฆ

By enrolling in this course, learners will gain essential knowledge and skills in regulatory risk management, enabling them to make informed decisions, reduce compliance risks, and drive business success. The course curriculum covers key topics such as global regulatory frameworks, risk management strategies, quality system regulations, and post-market surveillance. Upon completion, learners will be equipped with the necessary skills to excel in their careers, making them valuable assets in the medical device industry.

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ใ‚ณใƒผใ‚น่ฉณ็ดฐ

โ€ข Introduction to Medical Device Regulatory Risk Management
โ€ข Understanding Regulatory Frameworks for Medical Devices
โ€ข Identifying and Analyzing Regulatory Risks in Medical Devices
โ€ข Risk Management Strategies in Medical Device Development
โ€ข International Medical Device Regulations and Standards
โ€ข Role of Quality Management Systems in Regulatory Risk Management
โ€ข Regulatory Compliance for Medical Device Labeling and Promotion
โ€ข Clinical Evaluation and Post-Market Surveillance for Regulatory Risk Management
โ€ข Incident Management and Reporting in Medical Device Regulatory Risk Management
โ€ข Case Studies on Medical Device Regulatory Risk Management

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ใ‚ญใƒฃใƒชใ‚ข่จผๆ˜Žๆ›ธใ‚’ๅ–ๅพ—

ใ‚ตใƒณใƒ—ใƒซ่จผๆ˜Žๆ›ธใฎ่ƒŒๆ™ฏ
EXECUTIVE DEVELOPMENT PROGRAMME IN MEDICAL DEVICE REGULATORY RISK MANAGEMENT
ใซๆŽˆไธŽใ•ใ‚Œใพใ™
ๅญฆ็ฟ’่€…ๅ
ใงใƒ—ใƒญใ‚ฐใƒฉใƒ ใ‚’ๅฎŒไบ†ใ—ใŸไบบ
London School of International Business (LSIB)
ๆŽˆไธŽๆ—ฅ
05 May 2025
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