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Our experts provide medical device clients with leading strategic measurement services, qualitative and quantitative research and patient journey studies, PRO outcomes analyses, rare disease research, and PRO regulatory support services.

On medical device manufacturers

The FDA encourages the integration of patient-reported outcome (PRO) instruments in the development, evaluation, and surveillance of medical device studies. For medical device manufacturers, determining the best PRO for your study can be challenging, but QualityMetric’s scientific team can help.

Our team can use its decades of experience in the development, modification, validation, implementation, and analysis of PROs in more than 60 therapeutic categories to help you select or adapt a PRO. These experts provide our medical device clients with leading strategic measurement services, qualitative and quantitative research and patient journey studies, PRO outcomes analyses, rare disease research, and PRO regulatory support services.