Americans are privileged to have access to the safest — not to mention most advanced — pharmaceutical program in the world. From Provo, Utah to the East Coast, The U.S. Food and Drug Administration (FDA) is the primary authority on drug safety, and is responsible for not only evaluating new drugs, but for providing information...Read More

  In 1996, the U.S. Food & Drug Administration (FDA) approved the first transvaginal mesh device. The device was created to treat women with pelvic organ prolapse or “POP,” as it’s more commonly known. POP is a medical condition which causes pelvic organs to wander or drop out of place. In theory, transvaginal mesh was...Read More