The challenges and opportunities of leveraging patient-reported outcomes (PROs) to support device regulatory decisions are getting attention at FDA meetings this week. In this latest Market Pathways' Pick of the Week: some expert tips on PROs from consultant and former FDA reviewer Kevin Go.Read Article
Director, Industry Partnerships & Senior Market Analyst
20 Years of Experience
@Tracy_Schaaf's 20+ years of experience in the global medical device market analysis space brings a seasoned, multi-faceted perspective to the MedTech Strategist team. As a senior writer/market analyst, she contributes regularly to the company’s newest publication, MedTech Strategist Market Pathways: Global Regulatory, Reimbursement & Policy Review. Her coverage includes emerging regulatory, reimbursement, and market access trends, pioneering companies that are forging new pathways through the increasingly complex global medtech landscape, and the innovators who are working to bring novel, life-saving devices to market.
Tracy also developed and writes regularly for the popular “In MedTech History” series on the company’s Community Blog, where she highlights the trailblazing originators of today’s greatest medical device achievements. In addition, she manages MedTech Strategist’s important collaborations with top-tier global co-promotional partners including AdvaMed, the Irish Medtech Association, MedTech Europe, and many others across the device space.