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We look forward to seeing you in Barcelona!
Come to our booth and take the opportunity to get answers from our specialists about our featured products in mycology, serology, bacteriology, and quality control. You will also be able to get demos of our Unity software for Quality Control data management. You will be able to learn about the CFX opus, our new generation real-time PCR system, as well as our Geenius HIV/HCV confirmatory system.
Join us at the Innovation & Pipeline Theater
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| IVDR impact for molecular labs in health institutions |
| Speaker: | Prof Elizabeth Dequeker, PhD |
| Location: | Innovation Theater |
| Date/Time: | 27 April, 2024 at 14:30 |
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Since the entry into force in May 2022 of the IVDR regulation, the regulatory burden is becoming increasingly clear. This impact is also making itself known in molecular laboratories where, besides CE IVD kits, a lot of in-house IVD's are used. In this presentation we aim to clarify:
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The scope of the IVDR and the implications for commercially available CE IVDs |
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Use of in-House and this both for general reagents and controls as well as for in-House IVD assays |
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The practical implications of IVDR and how diagnostic labs can prepare for this |
Discover more from Bio-Rad
Whether you are a healthcare professional in a clinical, reference or public health laboratory or donor screening center, Bio-Rad has products to help you maximize efficiency and reliably detect pathogens in your patients. Explore our infectious disease diagnostics instruments, assays, reagents, and quality controls.
Infectious Disease Testing
Bio-Rad provides you with the systems, reagents and quality controls for bacteriology, mycology or serology testing to optimize your workflows and provide quality results.
Infectious Disease Quality Controls and Panels
Bio-Rad offers a wide range of infectious disease quality controls for both serology (antibody) and molecular (nucleic acid) testing. Our controls include tests for hepatitis and retrovirus as well as for sexually-transmitted, congenital, and respiratory diseases. They are compatible across platforms, meet international standards, and are manufactured according to the ISO 17511 standard. Long shelf lives help ensure performance of your assay and provide greater confidence in patient test results.
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