Whitepaper
Five IVDR challenges: What impact does IVDR have on your laboratory?
Discover the top challenges faced by laboratories and commercial manufacturers as they navigate the new regulatory framework for in vitro diagnostic medical devices. From increased training and resource requirements to documentation, risk mitigation, post-market surveillance, and justification of in-house developed tests, this whitepaper provides valuable insights into the key challenges and implications of IVDR compliance.
Learn how Devyser, a leading provider of IVD products, approaches the IVDR transition and encourages collaborative solutions with laboratories for patient safety.
Download the whitepaper now to stay informed and prepared for the upcoming changes.
Insight and inspiration
News | April 16, 2024
Devyser receives MDSAP certification for BrazilNews | Feb 20, 2024
Devyser Diagnostics AB publishes year-end report for January to December 2023News | Feb 06, 2024
Devyser strengthens its management team