Certificate in Medical Device Regulations for Quality Professionals

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The Certificate in Medical Device Regulations for Quality Professionals is a comprehensive course designed to empower quality professionals in the medical device industry. This program highlights the importance of regulatory compliance and quality systems, enabling learners to excel in their careers and drive success in their organizations.

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ใ“ใฎใ‚ณใƒผใ‚นใซใคใ„ใฆ

In an industry where meticulous adherence to regulations is paramount, this course is in high demand. It provides learners with the essential skills to navigate the complex landscape of medical device regulations, ensuring the safety and efficacy of products that improve patient care. Upon completion, learners will be equipped with a deep understanding of regulatory requirements, quality management systems, and best practices for medical device design, development, and manufacturing. By staying up-to-date with the latest industry standards and guidelines, professionals can advance their careers and contribute to the growth of their companies in the rapidly evolving medical device sector.

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ใ‚ณใƒผใ‚น่ฉณ็ดฐ

โ€ข
Medical Device Regulations Overview
โ€ข
Understanding Quality System Regulation (QSR)
โ€ข
ISO 13485: Medical Devices - Quality Management Systems
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Design Controls and Risk Management
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Change Management and Complaint Handling
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Medical Device Reporting and Adverse Event Management
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Clinical Data Management and Post-Market Surveillance
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Audit and Inspection Preparation
โ€ข
Regulatory Affairs and Submissions for Medical Devices

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ใ‚ตใƒณใƒ—ใƒซ่จผๆ˜Žๆ›ธใฎ่ƒŒๆ™ฏ
CERTIFICATE IN MEDICAL DEVICE REGULATIONS FOR QUALITY PROFESSIONALS
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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