Webinar
Learn about the latest regulatory updates impacting medical technology companies, industry insights and trends, nuances behind the headlines, and strategies for engaging with the FDA Center for Devices and Radiological Health from Mark Leahey, the president and CEO of the Medical Device Manufacturers Association (MDMA), a leading national trade association representing hundreds of innovative and entrepreneurial medical technology companies in Washington, D.C.
Sheridan Liaw
SLiaw@wsgr.com
Eva Yin, Ph.D., M.P.H., is a partner in Wilson Sonsini Goodrich & Rosati’s FDA regulatory, healthcare, and consumer products practice. Her practice includes conducting FDA and healthcare regulatory due diligence for corporate transactions; providing legal counsel to manufacturers regarding FDA approval/clearance for various products—including medical devices, mobile apps, and drugs, FDA compliance, regulation of promotional materials and labeling, and manufacturer compliance under federal and state healthcare laws, e.g., the federal Anti-Kickback Statute (AKS), False Claims Act (FCA), Sunshine Act, state licensing laws, corporate practice of medicine, etc.; reviewing contracts and compliance policies for manufacturers; and providing legal analysis and risk assessment of business models and fee arrangements involving patient assistance programs, healthcare professionals, or hospitals/clinics under federal and state healthcare laws and regulations.