Medical Device Risk Management Seminar (ISO 14971:2019)
Gstudy > Courses and seminars > Medical Device Risk Management Seminar (ISO 14971:2019)
Regulation
Quality Assurance
Location: Frontal
Starts at: 09:30
Duration: 1 Meeting
Language: Hebrew
This seminar focuses on providing practical knowledge and skills for effective risk management in medical devices, based on the ISO 14971:2019 standard.
It aims to comprehensively understand the latest regulatory requirements and the risk management process throughout the product lifecycle—from design to production and post-market activities.
Date & Hours - 20.10.2025 | 9:30-15:30
Haifa, Matam
About Sivan Luder, PhD
Dr. Sivan Luder is a Regulatory, Clinical, and Quality Expert with a PhD in Molecular Biology and over 10 years of experience across various industries, with a strong focus on the medical device sector. Possesses a deep scientific background and extensive experience in leading the development and implementation of medical devices from concept to commercialization, managing regulatory projects, and preparing...
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Registration Information
Early Bird Discount: 30 days in advance
Group Rates: Available for 3+ participants
Corporate Training: Custom programs for 8+ participants
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