The explosion of digital health and medical technology – including mobile health, health IT, wearables, telehealth/telemedicine, and personalized medicine – continues to revolutionize the ways in which health care services are delivered. With new players entering the space from big tech and other industries, it’s important to understand the vast and varied regulatory regimes to which digital health initiatives may be subject.
活动类型: 继续法律教育（CLE）或继续专业发展（CPD）, 网络研讨会
- 开始日期／时间:
- 23 January 2020, 12:00 PM ET
- 结束日期／时间:
- 23 January 2020, 1:00 PM ET
Join Reed Smith’s global Digital Health & MedTech team for this CLE webinar for a practical discussion on the scope and impact of health care and privacy regulation on the digital health industry. Topics will include:
- Federal and state health care regulatory and reimbursement issues, including fraud and abuse implications and insurance coverage for digital health devices and services
- Applicability of federal and state privacy laws, including the Health Insurance Portability and Accountability Act (HIPAA), Telephone Consumer Protection Act (TCPA), California Consumer Privacy Act (CCPA), biometric privacy laws, and Federal Trade Commission (FTC) and Office for Civil Rights (OCR) enforcement
- U.S. Food & Drug Administration (FDA) regulation, enforcement discretion, and risk-based approach to software functions found in many of today’s mobile medical apps and other digital health technology
- Global issues, including data, consumer protection, and the medical device regulatory framework in the European Union (EU) and other regions