Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course
A Service by SGS Indonesia
Description
This course will provide participants with an overview of the critical changes in relation to EU In Vitro Diagnostic Regulation, along with the implementation timescales.
Course Content:
An overview of the new regulation
The key changes you need to be aware of
What EU IVDR means in practice
Where you can find further information
A quiz to test your knowledge
This course is intended for, but not limited to, regulatory personnel, managers, CEO, CFO, or any medical device or IVD field personnel who want to learn about the new regulations.
The product we offer is a services and any disputes related to the services must be resolved directly with PT. SGS Indonesia.
All sales are final, and there will be no refunds provided for services purchased through our platform.
The SGS certificate is available to download once you have achieved a pass mark of 80% or more in the final assessment to complete this course.
The services purchased trough our platform are valid for 1 (one) year from the date of purchased.
The details on how to use or redeem the services will be provided in the order confirmation email sent to you upon successful purchase. Please carefully review this information, including any unique codes, instructions, or links provided.