Tag: Adverse event reporting

According to the FDA, dietary supplements are regulated under a different set of rules than prescription drugs, leading many to ask, "Does the FDA check supplements?". Manufacturers are primarily responsible for ensuring their supplements are safe before they hit the shelves.

Since the passage of the Dietary Supplement Health and Education Act (DSHEA) in 1994, the number of dietary supplements on the market has increased nearly twentyfold. This growth has brought increased scrutiny to the question of **how does the FDA regulate dietary supplements?**, a process that differs significantly from drug oversight and places the primary responsibility for safety on manufacturers.