Faculty Profile: Ramy Fayed

Ramy FayedDentons
Current TBA Courses

Ramy Fayed is a partner in the Health Care Practice Group in Dentons US LLP's Washington, D.C. office. He has been recognized by Super Lawyers, Nightingale's Healthcare News, and Best Lawyers as one of the leading health care lawyers in the US.  In his practice, he advises a broad range of health care organizations, including hospitals, academic medical centers and manufacturers of pharmaceuticals and medical devices on compliance with the federal health care program anti-kickback law, the Stark law, the False Claims Act, and Medicare and Medicaid compliance and reimbursement issues. He routinely counsels clients on requirements surrounding inpatient admissions, physician supervision requirements, billing rules for outpatient observation services, and issues related to "provider-based" status. Ramy provides strategic advice and assists clients in conducting internal reviews to evaluate the existence of potential overpayments, and to make appropriate self-disclosures and voluntary refunds to federal payors.

Ramy frequently counsels health care systems, technology companies, and other providers and suppliers on compliance with the HIPAA privacy, security, and breach notification requirements, as well as state and other requirements related to the confidentiality and security of data. He regularly works with clients to address privacy and security best practices and respond to data breaches and other privacy and security incidents. Ramy also provides strategic counseling on health care data use issues including data aggregation, data analytics, and de-identification.

Ramy also assists clients in responding to, and complying with, investigations and audits undertaken by federal and state regulatory and enforcement agencies. He also represents clients in administrative litigation, including Provider Reimbursement Review Board (PRRB) and administrative law judge (ALJ) appeals. He also represents academic medical centers and institutional review boards (IRBs) on clinical research-related issues, including drafting and revising human subject protection programs, policies and procedures relating to IRBs generally, IRB member and principal investigator conflicts of interest and the informed consent process.