V&V | Why, What, How

Medical devices industry Gsap
Gstudy > Courses and seminars > V&V | Why, What, How

Sep 7, 2022

By Ossie Milanov, B.A.

Regulatory

Location: Frontal

Starts at: 09:00

Duration: 6 hours

Language: Hebrew

This one day course is designed for all QA and RA staff and engineers in the medical device industry that are facing the challenge of defining the testing requirements for their device(s). This course is designed to give you the tools to making an informed decision regarding the testing and the ability to explain this decision in a manner acceptable to the regulatory authorities. 

Course date - 07/09/22

Course Hour's - 09:00-15:00

Location - Matam Haifa

Fee - 1,500 NIS + VAT

  • About Ossie Milanov, B.A.

    Ossie Milanov is a regulatory and quality expert. She has worked with many start up medical device companies over the years.  She has experience in establishing, implementing and maintaining a QMS; in particular effective and compliant Risk Management and Post Market Surveillance. Ossie has experience in preparing Regulatory Strategies and submissions for the FDA, EU and WHO. She has successfully participated in...

Comments

This one day course is designed for all QA and RA staff and engineers in the medical device industry that are facing the challenge of defining the testing requirements for their device(s). This course is designed to give you the tools to making an informed decision regarding the testing and the ability to explain this decision in a manner acceptable to the regulatory authorities.

Course date – 07/09/22

Course Hour’s – 09:00-15:00

Location – Matam Haifa

Fee – 1,500 NIS + VAT

For further information please contact Lital at 052-3610566 or Lital@gsap.co.il

 

 

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