概要
COURSE DESCRIPTION
The course contains the following elements:
- 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
Upon successful completion learners will be able to download a certificate of completion.
You will be granted 12 months access to this course, effective from the date of purchase.
目的
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.
対象者
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