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VRCI Verici Dx Plc

3.75
-0.25 (-6.25%)
31 Jan 2025 - Closed
Delayed by 15 minutes
Share Name Share Symbol Market Type Share ISIN Share Description
Verici Dx Plc LSE:VRCI London Ordinary Share GB00BM8HZD43 ORD GBP0.001
  Price Change % Change Share Price Bid Price Offer Price High Price Low Price Open Price Shares Traded Last Trade
  -0.25 -6.25% 3.75 3.50 4.00 3.875 3.75 3.875 113,328 15:48:09
Industry Sector Turnover Profit EPS - Basic PE Ratio Market Cap
Business Services, Nec 1.01M -8.73M -0.0360 -1.11 9.7M

Verici Dx PLC CLIA Certificate of Compliance update

20/07/2023 7:00am

RNS Non-Regulatory


TIDMVRCI

Verici Dx PLC

20 July 2023

Verici Dx plc

("Verici Dx" or the "Company")

CLIA Certificate of Compliance update

US clinical laboratory now fully accredited in 49 states

Verici Dx plc (AIM: VRCI), a developer of advanced clinical diagnostics for organ transplant, announces that further to the RNS dated 2 March 2023 , the Company has received compliance authorisation for the operation of its commercial clinical laboratory testing in respect of samples from an additional four US states, including the important addition of California , with the Company laboratory now fully accredited in a total of 49 states.

Together with the CLIA certification previously obtained from the Centers for Medicare & Medicaid ("CMS"), clinicians at transplant medical centres in these additional states are now enabled to order Verici Dx's transplant tests, expanding the Company's commercial reach. California has consistently accounted for over 10 per cent. of the national US volume of kidney transplant procedures in each year since 1998 and has conducted the highest volume of transplants by any state each year over the same period.

Verici Dx launched its first product, Tutivia(TM), for the detection of acute rejection in kidney post-transplant patients, in January 2023 and recently announced the successful validation of Clarava(TM), a first-in-class pre-transplant prognosis test for the risk of early acute rejection in deceased donor recipients, which it expects to launch later this year. The additional state accreditations provide further validation of Verici Dx's clinical laboratory for its tests to be used by transplant clinicians across the US.

The Company continues to work towards full accreditation in the final state of New York, which has its own compliance requirements .

The CLIA certification and additional state approvals further exemplify Verici's commitment to a quality-focused approach to providing advanced kidney transplant diagnostic services to clinicians and patients in need.

Sara Barrington, CEO of Verici Dx, said: " This is another important step in our strategy, expanding our commercial reach and making it easier for clinicians to order our tests helping to drive the adoption of both Tutivia(TM) and Clarava(TM) ."

Enquiries:

 
Verici Dx                                                        www.v ericidx .com 
Sara Barrington, CEO                                                Via Walbrook PR 
Julian Baines, Chairman 
 
Singer Capital Markets (Nominated                             Tel: +44 20 7496 3000 
 Adviser & Broker) 
Aubrey Powell / Sam Butcher 
 
Walbrook PR Limited                Tel: +44 20 7933 8780 or vericidx@walbrookpr.com 
Paul McManus / Stephanie Cuthbert                  Mob: +44 7980 541 893 / +44 7796 
 /                                                                        794 663 / 
 Sam Allen                                                            07502 558 258 
 

About Verici Dx plc www.vericidx.com

Verici Dx is a developer of a complementary suite of leading-edge tests forming a kidney transplant platform for personalised patient and organ response risk to assist clinicians in medical management for improved patient outcomes. The underlying technology is based upon artificial intelligence assisted transcriptomic analysis to provide RNA signatures focused upon the immune response and other biological pathway signals critical for transplant prognosis of risk of injury, rejection and graft failure from pre-transplant to late stage. The Company also has a mission to accelerate the pace of innovation by research using the fully characterised data from the underlying technology and collaboration with medical device, biopharmaceutical and data science partners.

The foundational research was driven by a deep understanding of cell-mediated immunity and is enabled by access to expertly curated collaborative studies in highly informative cohorts in kidney transplant.

This information is provided by Reach, the non-regulatory press release distribution service of RNS, part of the London Stock Exchange. Terms and conditions relating to the use and distribution of this information may apply. For further information, please contact rns@lseg.com or visit www.rns.com.

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END

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(END) Dow Jones Newswires

July 20, 2023 02:00 ET (06:00 GMT)

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