The FDA grants trans-inclusive at-home cervical screening device priority review
Briefly

For women, trans, and non-binary people, undergoing a regular cervical smear can be unpleasant due to the uncomfortable speculum, leading to gender-based discrimination in appointments.
The FDA granted Breakthrough Device Designation status for the Teal Wand, fast-tracking its review process, aiming to provide a more comfortable and inclusive cervical screening experience.
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