Vigilance Reporting – EU legislation

We have the pleasure to propose you a course on Vigilance Reporting for Medical Devices in the EU. We will present you with the full process and how to execute vigilance reporting. The 4 modules are made to help you accelerate your knowledge and be immediately ready to execute this task as soon as you finish the training.

eTraining Vigilance Reporting EU MDR and IVDR - Medical Devices

Course Information

Categories:

Course Instructor

Monir EL Azzouzi Monir EL Azzouzi Trainer

eTraining Vigilance Reporting – EU Requirements

SALE 49,00

What Others Have Said

Excellent training
By: Dana Tirosh

useful tools and practicable examples. Easy to understand. Thank You!

Excellent training
By: Lydia Bedre-dine

My 2nd training with EMD, and still so satisfied. The instructor gives useful tools and practicable examples. Easy to understand and covered all my questions. Thank you!


2 thoughts on “Vigilance Reporting – EU legislation”

  1. Thanks for this mini-course on vigilance reporting. It helps in a quick manner to remember all the basic notions of the vigilance system under MDR 2017/745. The section ‘trend reporting’ was very useful. thank you, Monir!

  2. Ceren Alemdaroglu

    That was a very insightful training covering the main topics in Vigilance Reporting with references and links. Thank you, Monir!

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