Medical Device Risk Management Seminar

Medical devices industry Gsap
Gstudy > Courses and seminars > Medical Device Risk Management Seminar

Jul 16, 2025

By Sivan Luder, PhD

Regulation

Quality Assurance

Location: Frontal

Starts at: 09:00

Duration: 1 Meeting

Language: English

Medical Device Risk Management Seminar (ISO 14971:2019) :

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

16.07.2025

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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