We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
Vicotex

Download Mobile App




Rapid HSV-2 Test Sets New Standard in STI Diagnostics

By LabMedica International staff writers
Posted on 28 Jul 2025

With an estimated 65 million Americans living with genital herpes and around 90% of those undiagnosed, there is an urgent need for faster, more efficient, accurate, and accessible testing methods. More...

Existing diagnostics, such as ELISA tests, commonly yield 17–22% equivocal results, resulting in misdiagnosis and delays in care. Specificity can be as low as 39.8% for certain index values, underscoring the inadequacy of current diagnostic tools. Such limitations often lead to uncertainty, distress, and postponed treatment, worsening patient outcomes. Now, a new rapid test for herpes simplex virus type 2 (HSV-2) addresses the limitations in STI diagnostics with its improved speed, accuracy, and accessibility.

Bio-Diagnostics Ltd.’s (Worcestershire, UK) HSV-2 BioCard test detects circulating antibodies to HSV-2 in the blood, indicating an active or past infection. Unlike HSV-1, which typically causes cold sores but can also lead to genital sores, HSV-2 is the primary cause of genital herpes, making accurate differentiation essential for treatment and limiting transmission. Bio-Diagnostics initially developed the BioCard HSV-2 testing technology as an accessible screening method to detect undiagnosed infections of genital HSV-2, but was later recommended by healthcare protection agencies to confirm around 20% of results that are left unclear by standard methods. The BioCard platform is also modular, supporting other diagnostic applications such as infectious diseases, autoimmune markers, toxins, and food safety.

The technology has been validated using blinded panels from UKHSA and MHRA NIBSC, demonstrating up to 100% sensitivity and 99.5% specificity for COVID-19 immunity tracking—further proving the reliability of the BioCard platform. It is the only technology to correctly identify every single UK NEQAS sample since its launch. Use of testing technologies by following the CDC guidelines resolves the compound effects of misdiagnosis, distress, and delayed care. The BioCard HSV-2 Rapid Test bridges this critical gap with point-of-care accuracy, simplicity, and global scalability. The BioCard HSV-2 test is typically administered in clinical settings or testing facilities by healthcare professionals, ensuring accurate diagnosis alongside access to supportive care. Bio-Diagnostics is now seeking new distribution partners and technology licensing collaborators to expand access across clinical, public health, and remote care settings.

Related Links:
Bio-Diagnostics Ltd


Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Electrolyte Analyzer
CBS-4000 (CBS-400)
Manual Pipetting Aid
Pipette Controllers macro
Electrolyte Analyzer
BKE-B
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Clinical Chemistry

view channel
Image: New findings demonstrate that anti-Müllerian hormone (AMH) may help identify which breast cancer patients are most likely to benefit from chemotherapy plus endocrine therapy (Image Credit: Shutterstock)

AMH Test Helps Predict Adjuvant Chemotherapy Benefit in Premenopausal Breast Cancer

Hormone receptor-positive, human epidermal growth factor receptor 2-negative (HR+/HER2-) breast cancer can present a difficult treatment decision in premenopausal patients with low recurrence scores.... Read more

Microbiology

view channel
Image: The QIAstat-Dx BCID GPF Plus AMR Panel is the first QIAstat-Dx panel for bloodstream infections to receive FDA clearance (Photo courtesy of Qiagen)

FDA Clears One-Hour Panel for Bloodstream Infection and AMR Detection

Bloodstream infections can rapidly progress to sepsis, a life-threatening condition affecting an estimated 1.7 million adults in the U.S. each year. Rapid identification of pathogens and antimicrobial... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.