A new vaccine that combines flu and COVID-19 protection in one shot shows promising results, but the U.S. Food and Drug Administration (FDA) says it wants more data before it can be approved.

The Food and Drug Administration has approved the first at-home ... said the FDA’s decision was based on a study in more than 600 women that showed self-collected samples using its test had ...

The maker of an at-home cervical cancer screening test said Friday it has won approval ... “That’s why this FDA approval means so much; it’s not just about an innovative new product, it ...

(Reuters) - The U.S. Food and Drug Administration has approved the first at-home ... FDA's decision was based on a study in more than 600 women that showed self-collected samples using its test ...

The Food and Drug Administration on Friday approved the first at-home test to screen ... Wand is not the first HPV test that uses a vaginal sample: Last year, the FDA approved a similar swab ...

On Friday, May 9, the FDA approved the Teal Wand ... the Teal Wand will allow individuals with uteruses to test for human papillomavirus, or HPV, at home. HPV is one of the leading causes of ...