Join us for our webinar on the European In Vitro Diagnostics Regulation (IVDR) on Thursday, May 25 at 17:00 CEST.
The IVDR has now been in use for about a year. For this reason, we would like to take a look at experiences to date and current challenges for everyday laboratory work. Gain insights into the implementation of the IVD regulation for Next-Generation Sequencing analyses through a field report by Dr. Michaela Ihle, the Quality Management Officer for Pathology at the University Hospital Cologne. Discuss with Dr. Ihle and our Head of Quality Management, Dr. Niels Bojunga, what laboratories and industry can learn from each other.
Take the opportunity to exchange experiences. Discuss the following topics with our experts:
- What impact does the IVDR have on Laboratory Developed Tests (LDTs)?
- How to define an LDT under IVDR?
- How to implement a risk management and performance evaluation strategy?
- What are the resource requirements under IVDR?
- What are the benefits of a standardized approach through networking?
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