概要
Delegates participating in this course will:
- Gain an overview of the critical changes with EU MDR and EU IVDR, and their implications
- Find out about implementation timescales and their impact on resources
- Discover what EU MDR and EU IVDR mean in practice
目的
About the EU MDR and EU IVDR
The EU MDR and EU IVDR were published in the Official Journal of the European Union on May 5, 2017 as Regulation (EU) 2017/745 and Regulation EU (2017/746). The new rules will apply after a transition period of three years for MDR and five years for IVDR. These two eLearning courses will help medical device and In Vitro diagnostic device manufacturers understand the complex new regulations.
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.
バンドルコンポーネントのそれぞれに対してオファリングを選択し、下の[カートに追加]ボタンをクリックします。
Introduction to the New EU Medical Device Regulation (MDR) eLearning Course
目的
This course will provide participants with an overview of the critical changes in relation to EU Medical Device 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
提出物
Introduction to the New EU Medical Device Regulation (MDR) eLearning Course
Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course
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
提出物
Introduction to the New EU In Vitro Diagnostic Regulation (IVDR) eLearning Course
