Eurofins Biomnis has a large team of IT specialists which allows us to build proprietary systems in-house and adapt them to suit the evolving needs of clients. Orcis, our electronic test ordering system is now in use by over 500 doctors and nurses and has been used to order 1.2m tests since January 1st. It… Read more »
Recently we read about exciting test research from the Tallaght Institute of Memory & Cognition, St James’s Hospital and Trinity College Dublin, to detect Alzheimer’s Disease. We eagerly await updates. On the Eurofins front we are delighted to let you know of the following new tests; 1. The Environmental Cocktail Blood test. Coming September 2025…. Read more »
Suited for laboratories of all sizes, the OsmoPRO MAX revolutionizes osmolality testing with innovative flow-through technology that eliminates the need for consumables by pipetting samples directly from primary tubes, performing testing and cleaning within the device. Continuous loading and unloading removes the need to batch test. Experience unparalleled automation, workflow flexibility, and data management combined… Read more »
Ana, Clinical Biochemistry Section Lead at Bedfordshire Hospitals NHS Foundation Trust, reveals how they leveraged ValidationManager software solution to complete a major replacement of their Roche modular analyzers, with over 100 assays involved — effortlessly and within tight schedules.
Genseq are delighted to launch our IS015189:2022 accredited single gene testing service. Genseq’s ISO15189:2022 accredited single gene tests are based on a CE-IVD marked qPCR and high-quality sanger sequencing. We currently offer a variety of single gene tests including, DPYD, TPMT, CPY2C19, HFE, and TTR for pharmacogenomic and inherited disease testing (see our website for full details: genseqgroup.com).
Genseq are delighted to launch 11 new IS015189:2022 accredited hereditary cancer panels. Genseq offer a range of Hereditary Cancer gene panels (see our website for full details: genseqgroup.com). These are in silico panels based on whole exome sequencing (WES) data. All panels include single nucleotide variants (SNV), small insertions/deletions (indels), and copy number variation (CNV)… Read more »