HISTOPATHOLOGY
Fast, very fine, precise, and homogenous staining. Precision immunohistochemistry inseparable from precision oncology
Eric Bonte, Pathologist, Le Centre Médical De Pathologie De Compiègne
of advanced staining of formalin-fixed paraffin wax-embedded tissue, as well as advanced capillary gap technology for whole-slide coverage. The 30 fully independent stations allow maximum flexibility with limited downtime, and nullify splitting and sorting of cases, while the predictable turnaround time of two hours and 45 minutes for all biomarkers supports an efficient workflow. On the business side, a partnership with GenieOnline powers auto-replenishment for worry-free stock maintenance, while pay-per-slide and transparent cost management keeps costs under control.
Sakura Finetek is a recognised
and reliable partner with many years of innovative presence in the pre-analytical segment. The company’s vision is to fully automate the laboratory by empowering pathologists and technologists worldwide. Its unique SMART Automation approach has helped laboratories to attain a higher quality diagnostic process, consistent results, and a reduction in rework, thus keeping up with rising cancer cases. The SMART Automation concept covers all stages of the pre-analytical process and now Sakura can extend this approach into advanced IHC staining.
References 1 Chadwick L. Cancer cases expected
to grow by more than 20% in Europe by 2045 - WHO agency. Euronews 2024 (
https://www.euronews.com/ health/2024/02/01/cancer-cases- expected-to-grow-by-more-than-20-in- europe-by-2045-who-agency)
2 National Pathology Programme. Digital First: Clinical Transformation through Pathology Innovation. NHS England 2014 (https://www.england.nhs. uk/2014/02/npp-digital-first/)
3 Nielsen S, Bzorek M, Vyberg M, Røge R. Lessons Learned, Challenges Taken, and Actions Made for “Precision” Immunohistochemistry. Analysis and Perspectives From the NordiQC Proficiency Testing Program. Appl Immunohistochem Mol Morphol.
2023;31(7):452-458. doi:10.1097/ PAI.0000000000001071
4 European Union. Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices. EUR- Lex 2017 (
https://eur-lex.europa.eu/eli/ reg/2017/746/2024-07-09)
5 Bank PCD, Jacobs LHJ, van den Berg SAA et al. The end of the laboratory developed test as we know
it? Recommendations from a national multidisciplinary taskforce of laboratory specialists on the interpretation of the IVDR and its complications. Clin Chem Lab Med. 2020 Nov 23:cclm-2020-1384. doi: 10.1515/cclm-2020-1384. Online ahead of print.
6 Truumees B, Kristoffersen HL, Julio TWH, Rasmus Røge R, Nielsen S. Improving the Quality of IHC: Impact of Tailored Advice and Reassessment After a Failed External Quality Assessment Result. Poster session presented at: USCAP 113th Annual Meeting; 2024 Mar 23-28; Baltimore, MD, USA. (
https://www.nordiqc.org/ downloads/documents/200.pdf)
For more information on the Tissue Tek Genie system visit the website:
www.sakura.eu/solutions/advanced- staining/genie
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