Executive Development Programme in Scaling ISO 13485

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The Executive Development Programme in Scaling ISO 13485 is a comprehensive course designed to meet the growing industry demand for professionals with expertise in medical device quality management systems. ISO 13485 certification is essential for organizations involved in the design, production, installation, and servicing of medical devices.

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This programme provides learners with the knowledge and skills necessary to implement and manage a quality management system that complies with ISO 13485 requirements. Through a combination of lectures, case studies, and interactive exercises, learners will gain a deep understanding of the regulatory and quality requirements for medical devices. They will also develop essential skills for career advancement, including leadership, communication, and project management. By completing this programme, learners will be able to demonstrate their commitment to quality and regulatory compliance, setting themselves apart in a competitive job market. With the global medical device market projected to reach $612.7 billion by 2025, there has never been a better time to invest in this valuable certification.

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โ€ข Introduction to ISO 13485 & its importance in medical devices
โ€ข Understanding the requirements of ISO 13485:2016
โ€ข Best practices for implementing ISO 13485 in an organization
โ€ข Risk management in scaling ISO 13485
โ€ข Strategies for maintaining compliance during growth and expansion
โ€ข Management responsibility and resource management in scaling ISO 13485
โ€ข Measurement, analysis, and improvement of the QMS in a scaling organization
โ€ข Handling of customer feedback and complaints in scaling ISO 13485
โ€ข Internal audits and management review in scaling ISO 13485

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EXECUTIVE DEVELOPMENT PROGRAMME IN SCALING ISO 13485
ๆŽˆไบˆ็ป™
ๅญฆไน ่€…ๅง“ๅ
ๅทฒๅฎŒๆˆ่ฏพ็จ‹็š„ไบบ
London School of International Business (LSIB)
ๆŽˆไบˆๆ—ฅๆœŸ
05 May 2025
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