Risk Management Seminar
Gstudy > Courses and seminars > Risk Management Seminar
Quality
Regulatory
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 deliver a comprehensive understanding of the latest regulatory requirements and the risk management process throughout the product lifecycle—from design to production and post-market activities.
Date & hours:
05.03.2025
09:30-15:30
Location; Matam Haifa
Price - 1,500 NIS + VAT
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...
Contact Us
Thank you for registering to the course!
We will contact you soon in order to complete the registration procces.
In the meantime, the course details have been emailed to you.
Comments
The aim of this seminar is to provide concise but complete knowledge and skills required for medical device risk management, according to ISO14971:2019.