Scott Thiel is a director in Guidehouse's Healthcare and life sciences disputes, regulatory, compliance, and investigations practice, leading the health information technology regulatory group. Scott has over two decades of experience in the medical device industry, with expertise including product development, software, and connectivity related to medical devices (including interfaces with consumer electronics), regulatory affairs, compliance, and quality system creation and remediation.
Scott has been very active in industry groups, assuming leadership roles within the Continua Health Alliance; acting as a representative at AdvaMed in the software and infusion pump working group at AAMI during the creation of AAMI/ANSI SW 68 and IEC 62304; helping conceive, organize, facilitate, and execute the FDA-Continua-CIMIT co-sponsored three-day workshop at FDA to discuss interoperability of medical devices; assuming leadership roles in the Medical Device Interoperability Safety Working Group; and participation in the mHealth Regulatory Coalition and Clinical Decision Support Coalition. Scott is a regularly invited speaker at conferences and workshop nationwide.
MBA, Indiana Wesleyan University BS, Biology/Chemistry, Ball State University