Qvin™ Introduces Q-Pad™: Transforming Women's Health with FDA-Cleared Lab Testing using Menstrual Blood
SAN FRANCISCO, Jan. 8, 2024 /PRNewswire/ -- Qvin™, the biotechnology research company that developed the first and only healthcare service that collects menstrual blood samples as an alternative to traditionally collected venous blood draws, today announced FDA clearance of its Q-Pad™ and A1c Test. The clearance makes it possible for the millions of women in America who live with diabetes to receive monitoring of A1c, using laboratory tests performed on the Q-Pad. More broadly, this marks an opportunity for testing important biomarkers for the more than 80 million people who menstruate in the U.S.
- The traditional methods of blood testing require invasive procedures administered by medical professionals, and those can be time-consuming and expensive.
- And yet, menstrual samples had never previously been explored as a diagnostic source for health information.
- "Utilizing menstrual samples, the Q-Pad can address critical women's health issues that have historically been neglected," stated Søren Therkelsen, Co-founder of Qvin.
- "For instance, women seeking to understand their fertility status can soon monitor various reproductive hormones via menstrual blood using the Q-Pad.