Fit-for-Purpose COA Development: 25 years developing, modifying and validating PROs in more than 60 therapeutic categories. LEARN MORE
Translation Services: 25 years developing linguistically validated translations of COAs, CRFs, protocols, manuals, etc… READ MORE
QualityMetric By The Numbers: 41,000,000+ Global Survey administrations, 40,000+ Peer-reviewed articles across 100+ conditions, 2,000+ Language translations by mode of administrations, 100+ Condition-Specific, Country-Specific, and Insurance Claims Benchmarks General Population Norms. Which survey should you use? SEE OUR SUITE OF PRO SURVEYS
ePRO & EDC Integration: Seamless integration for optimal efficiencies using Web Service Application Programming Interface (API), Single Sign-on Access (SSO) or Electronic-Friendly Survey Administration. FIND OUT HOW
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.
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.
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