The FDA has approved three self-administered tests for the high-risk strains of HPV known to cause most cervical cancers.

Since 2024, the U.S. Food and Drug Administration has approved three self-collected HPV tests: Two are done in medical ...

The recommendation comes after the first at-home test, a self-swab, received federal approval earlier this year.

Most women prefer to complete HPV tests at home as long as the results are as accurate as those conducted by a clinician, ...

Guidelines expanded to include self-collection for HPV testing and revised guidance for exiting cervical cancer screening.

One of the first tests that allows patients to self-collect samples to screen for human papillomavirus (HPV) will soon be available in doctors' offices. In May, the U.S. Food and Drug Administration ...