Executive Development Programme in ISO 13485 Innovation

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The Executive Development Programme in ISO 13485 Innovation is a certificate course designed to equip professionals with the necessary skills to drive innovation in the medical device industry. This program is crucial in the current industry landscape, where there is a high demand for experts who can implement and manage ISO 13485 quality management systems.

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By completing this course, learners will gain a deep understanding of the standard and how to use it to foster innovation, reduce waste, and improve overall performance. The course covers key topics such as risk management, design control, and regulatory affairs, and provides learners with hands-on experience in applying these concepts in real-world scenarios. Upon completion, learners will be able to demonstrate their expertise in ISO 13485 and their ability to lead and manage innovation initiatives in the medical device industry. This course is an excellent opportunity for professionals looking to advance their careers and make a meaningful impact in the field.

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โ€ข Introduction to ISO 13485 & Medical Device Innovation
โ€ข Understanding ISO 13485:2016 Requirements
โ€ข Implementing ISO 13485: Quality Management System for Medical Devices
โ€ข Innovation in Medical Device Design & Development
โ€ข Risk Management in Medical Device Innovation
โ€ข Regulatory Affairs & Compliance for ISO 13485
โ€ข Human Factors & Usability Engineering in Medical Device Design
โ€ข Case Studies: Successful ISO 13485 Innovation Projects
โ€ข Change Management & Continuous Improvement in ISO 13485
โ€ข Strategic Planning for ISO 13485 Executive Development

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