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OraQuick® HCV Rapid Antibody Test - not proceeding

A single use, point-of-care test for the qualitative detection of antibodies to hepatitis C virus (HCV) in oral fluid, fingerstick whole blood, venipuncture whole blood, plasma and serum.

If you wish to be alerted to developments regarding this technology, including consultations and the release of NICE guidance, please express your interest by send an e-mail to medtech@nice.org.uk for the attention of the topic project manager.

Status: Suspended
Expected date of issue: TBC
Notification date: October 2010
Topic area:
  • Diagnostic procedures
  • Digestive system
  • Infectious diseases
 

NICE project team

Patient Involvement Lead: Laura Norburn
Analyst: Sarah Baggaley
Communications Lead: Tonya Gillis
Project manager: Marlon Hope
Implementation Lead: Katie Worrall
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Provisional schedule

Submission Date: TBC
Topic Selection: 16 December 2010
Draft guidance meeting TBC
Consultation opens: TBC
Consultation ends: TBC
Final guidance meeting: TBC
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Stakeholders

To be confirmed

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Project history

Date Update
5 August 2011 NICE's assessment of this medical technology is suspended. 
29 June 2011 NICE is unable to develop medical technology guidance on OraQuick HCV Rapid Antibody Test because the manufacturer has decided not to pursue a submission for evaluation to the Medical Technologies Evaluation Programme (MTEP).  NICE will therefore not be developing guidance on this topic.
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Key documents

This page was last updated: 28 March 2012

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Selected, reliable information for health and social care in one place

Accessibility | Cymraeg | Freedom of information | Vision Impaired | Contact Us | Glossary | Data protection | Copyright | Disclaimer | Terms and conditions

Copyright 2014 National Institute for Health and Care Excellence. All rights reserved.