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FDA updates biosimilar rules to cut costs and speed access to lower-priced biologic drugs.
The FDA released draft guidance to streamline biosimilar development by reducing unnecessary pharmacokinetic testing and allowing use of foreign clinical data, potentially cutting costs by up to 50% and speeding access to lower-priced biologic treatments for conditions like cancer and autoimmune diseases.
The agency is withdrawing its 2015 guidance, reflecting updated scientific experience from reviewing 82 approved biosimilars since 2009.
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La FDA actualiza las reglas biosimilares para reducir costos y acelerar el acceso a medicamentos biológicos de menor precio.