Professional Certificate in Device Post-Market Surveillance Report

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The Professional Certificate in Device Post-Market Surveillance Report course is crucial for professionals in the medical device industry. This course addresses the increasing demand for expertise in post-market surveillance, a critical aspect of device regulation and safety.

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Throughout the program, learners will develop essential skills in monitoring device performance, identifying and analyzing adverse events, and generating comprehensive surveillance reports. These skills are vital for ensuring device compliance with regulatory standards and promoting patient safety. By earning this certificate, professionals can demonstrate their commitment to industry best practices and advance their careers in medical device regulation, quality assurance, and clinical research. Furthermore, the course equips learners with the knowledge and tools to effectively contribute to post-market surveillance efforts and positively impact public health.

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โ€ข Unit 1: Introduction to Device Post-Market Surveillance Report
โ€ข Unit 2: Regulatory Framework for Medical Device Post-Market Surveillance
โ€ข Unit 3: Risk Management in Post-Market Surveillance
โ€ข Unit 4: Data Collection and Analysis for Post-Market Surveillance
โ€ข Unit 5: Adverse Event Reporting and Management
โ€ข Unit 6: Post-Market Clinical Follow-up Studies
โ€ข Unit 7: Periodic Safety Update Reports
โ€ข Unit 8: Corrective and Preventive Actions in Post-Market Surveillance
โ€ข Unit 9: Quality Management System for Post-Market Surveillance
โ€ข Unit 10: Best Practices in Medical Device Post-Market Surveillance

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ใ‚ตใƒณใƒ—ใƒซ่จผๆ˜Žๆ›ธใฎ่ƒŒๆ™ฏ
PROFESSIONAL CERTIFICATE IN DEVICE POST-MARKET SURVEILLANCE REPORT
ใซๆŽˆไธŽใ•ใ‚Œใพใ™
ๅญฆ็ฟ’่€…ๅ
ใงใƒ—ใƒญใ‚ฐใƒฉใƒ ใ‚’ๅฎŒไบ†ใ—ใŸไบบ
UK School of Management (UKSM)
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05 May 2025
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