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Results: 1-10 of 551

Evolving Patent Eligibility Standard for Computer-Implemented Inventions
  • McDermott Will & Emery
  • USA
  • September 23 2016

While addressing the patent eligibility of computer-implemented inventions, the US Court of Appeals for the Federal Circuit concluded that under step


Privileged Materials Provided Without Taxpayers’ Consent Should Not Waive Privilege
  • McDermott Will & Emery
  • USA
  • September 16 2016

In today’s tax environment and with the potential monetary awards to whistleblowers under Internal Revenue Code (Code) Section 7623, taxpayers are


FTC Weighs-in on Telehealth, Comments on Delaware’s Occupational Therapy Practice Rule
  • McDermott Will & Emery
  • USA
  • September 15 2016

On August 3, 2016, the Federal Trade Commission (FTC) staff submitted public comments regarding the Delaware Board of Occupational Therapy Practice’s


OIG Work Plan: A Roadmap to Identify Health Care Compliance Risk
  • McDermott Will & Emery
  • USA
  • September 2 2016

Each year, the US Department of Health and Human Services (HHS) Office of Inspector General (OIG) issues a Work Plan that summarizes new and ongoing


Augmented Reality
  • McDermott Will & Emery
  • USA
  • August 25 2016

If you haven’t heard about newest gaming craze yet, it’s based on what is called “augmented reality” (AR) and it could potentially impinge on your


Managing the Transition to Transformation: ProviderPayor Integration: 2016 Is Not the 1990s
  • McDermott Will & Emery
  • USA
  • August 17 2016

McDermott’s Managing the Transition to Transformation series is designed to help health systems and other health care industry leaders address the


Governance Oversight of Cybersecurity
  • McDermott Will & Emery
  • USA
  • August 16 2016

Most health system governing boards have some basic awareness of the cybersecurity issues that confront their organizations. Two recent developments


Does Digital Health Need Reimbursement?
  • McDermott Will & Emery
  • USA
  • August 16 2016

One of the most talked about topics when it comes to digital health is the reimbursement under various third-party payer programs. Most notably


FDA and OHRP Issue Joint Draft Guidance on IRB Written Procedures
  • McDermott Will & Emery
  • USA
  • August 15 2016

On August 2, 2016, the US Food and Drug Administration (FDA) and the Office for Human Research Protections (OHRP) jointly issued draft guidance


FDA Publishes Long-Awaited Draft Guidance on 510(k) Requirements for Modified Devices
  • McDermott Will & Emery
  • USA
  • August 10 2016

On August 5, 2016, the US Food and Drug Administration (FDA) posted two long-awaited draft guidance documents intended to help industry and FDA staff