Don’t miss our e-learning on IVDR implementation strategies.
In a series of 9 sessions we will help you to understand how the new IVDR will affect your product.
Within this e-learning you will learn how to efficiently update your Technical Documentation, how to handle the need for adapted and/or new reports and how to incorporate the new requirements into your existing structures.
More topics to be covered in the upcoming and previous sessions
- Implementation Strategies for IVDR – Timelines and Priorities – Work Packages
- When Medical Devices and IVDs meet REACH
- Classification under IVDR
- Economic operators and regulatory functions under IVDR
- Performance evaluation and clinical evidence under the IVDR
- Post market surveillance and vigilance under the IVDR
- EUDAMED and UDI under IVDR
After confirmation of your registration by knoell Germany GmbH, you will receive a link and an access code. From the time you receive the access code, the link to the e-learning video is valid for 56 days. The video can only be accessed five times during this period.