Medical Devices Virtual Public Meeting – Patient-Reported Outcomes (PROs) and Medical Device Evaluation

Patient-Reported Outcomes and Medical Device Evaluation

The U.S. Food and Drug Administration (FDA) is announcing a virtual public meeting entitled “Patient-Reported Outcomes (PROs) and Medical Device Evaluation: From Conception to Implementation”. The purpose of this public meeting is to discuss the benefits and challenges of incorporating the patient perspective in regulatory decision making using patient-reported outcome (PRO) instruments.

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