The U.S. Food and Drug Administration has approved a kit that will allow women to collect their own vaginal sample for HPV ...
For the first time, women in the United States have the ability to self-collect a sample to screen for human papillomavirus ...
The FDA has given the green light to a self-collection solution to test for HPV, making it one of the easiest options ...
The US FDA has approved a human papillomavirus (HPV) self-sampling solution developed by Roche that allows patients to ...
The FDA has approved a kit that will allow women to collect their own vaginal sample for HPV screening, a move that could increase early detection in those at risk of cervical cancer.
The FDA approved a new self-collection test to detect human papillomavirus (HPV) and identify women at risk for cervical ...
, opens new tab on Wednesday said the US Food and Drug Administration (FDA) has approved its human papillomavirus (HPV) ...
The FDA has approved two diagnostic devices that allow women to collect vaginal samples themselves for cervical cancer ...
Roche’s human papillomavirus solution is reportedly one of the first of its kind to be available in the United States.
The cost of a self-screen will be the same as the pelvic exam, Andrews said, because the sample is sent to a lab, which ...
Most primary-care physicians do not test for HPV. Typically, it’s performed by gynecologists, who collect samples for an HPV ...
Instead of a traditional speculum-involved pelvic exam to screen for cervical cancer, the US Food and Drug Administration has ...