Preferential Treatment: US FDA Asks Patients For Their Input

As the agency continues to incorporate more patient-preference data into its regulatory process, it is asking stakeholders on the kinds of diseases and other factors it should consider when evaluating patient-preference information. The feedback is ultimately meant to inform regulators and sponsors about what patients want as they develop products.

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Michael McCaughan (left) speaking with CDRH Director Jeff Shuren at the Reagan-Udall Foundation for FDA on 2 May. • Source: Ferdous Al-Faruque

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