Verici Dx plc, through its subsidiary Verici Dx Inc, develops prognostic and diagnostic tests for kidney transplant patients in the United Kingdom and the United States. Its products include Tutivia, a post-transplant diagnostic test for acute cellular rejection including sub-clinical rejection; Clarava, a pre-transplant prognosis test for early acute rejection risk; and Protega, a liquid biopsy predicting fibrosis and long-term graft failure risk. The company also offers sequencing services for tumor-only, tumor-normal, and germline exomes, whole transcriptome, targeted RNASeq and ncRNAs, and functional binding multicell assays, as well as bioinformatics and data science services. It collaborates with One Lambda Inc. on pre-transplant risk assessment (PTRA), The Westmead Institute for Medical Research on graft loss factors, and FBB Biomed, Inc. on research-use-only tests for neurologic diseases. Incorporated in 2020, Verici Dx plc is headquartered in Cardiff, United Kingdom.