Executive Development Programme in MedTech Regulatory Updates

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The Executive Development Programme in MedTech Regulatory Updates is a certificate course designed to provide learners with the latest regulatory developments in the medical technology industry. This programme emphasizes the importance of staying updated with regulatory changes to ensure compliance, minimize risks, and drive innovation in MedTech.

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With the increasing demand for professionals who can navigate the complex regulatory landscape, this course equips learners with essential skills to advance their careers in this rapidly evolving field. The course content includes global regulatory trends, clinical trial regulations, product approval processes, and post-market surveillance. Learners will gain hands-on experience in interpreting and applying regulations to real-world scenarios, fostering a comprehensive understanding of the regulatory landscape. By completing this programme, learners will demonstrate their expertise in regulatory affairs, positioning them for career advancement in the MedTech industry.

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่ฏพ็จ‹่ฏฆๆƒ…

โ€ข MedTech Regulatory Updates Overview
โ€ข Global MedTech Regulatory Landscape
โ€ข European Medical Device Regulation (MDR) & In Vitro Diagnostic Regulation (IVDR)
โ€ข US Food and Drug Administration (FDA) Regulations for Medical Devices
โ€ข Regulatory Requirements for Software as a Medical Device (SaMD)
โ€ข Clinical Evaluation and Post-Market Surveillance
โ€ข Quality Management Systems for MedTech Companies
โ€ข MedTech Regulatory Submissions & Documentation
โ€ข Global Harmonization & International MedTech Regulations
โ€ข Emerging Trends in MedTech Regulatory Affairs

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็คบไพ‹่ฏไนฆ่ƒŒๆ™ฏ
EXECUTIVE DEVELOPMENT PROGRAMME IN MEDTECH REGULATORY UPDATES
ๆŽˆไบˆ็ป™
ๅญฆไน ่€…ๅง“ๅ
ๅทฒๅฎŒๆˆ่ฏพ็จ‹็š„ไบบ
London School of International Business (LSIB)
ๆŽˆไบˆๆ—ฅๆœŸ
05 May 2025
ๅŒบๅ—้“พID๏ผš s-1-a-2-m-3-p-4-l-5-e
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