7,178 results found

On May 29, 2008, the Centers for Medicare & Medicaid Services (CMS) published a favorable Stark Law Advisory Opinion on an information technology arrangement.

On January 22, the Food and Drug Administration issued a draft industry guidance outlining the FDA's recommendations to the medical device industry with respect to addressing postmarket cybersecurity risks to patients.

On June 28, 2012, the United States Supreme Court ruled on the constitutionality of the Patient Protection and Affordable Care Act of 2010 (ACA) when it decided National Federation of Independent Business v. Sebelius.

Electronic health records (EHRs) replace traditional paper medical records with computerized recordkeeping to document and store patient health information.

On April 11, 2023, the Department of Health and Human Services through the Office of Civil Rights (OCR) announced that the Notifications of Enforcement Discretion issued under the Health Insurance...

Going forward, ONC will allow health developers to self-declare their products' conformance with 30 of the 55 certification criteria.

As part of its four-part Digital Health webinar series, on April 14, 2015, McDermott Will & Emery presented "Telehealth: Implementation Challenges in an Evolving Dynamic."

Fenwick & West hosted its annual Digital Health Investor Summit, bringing together investors, entrepreneurs and innovators interested in digital health.

The Internet of Medical Things (IoMT) is a hot topic in the world of medical devices. This summer, at the MedTech conference in Philadelphia, IoMT was the word on everyone's lips.

On Oct. 27, 2015, the Annual Meeting of the Illinois Association of Healthcare Attorneys was held at Navy Pier in Chicago. Hundreds of health care attorneys attended, including several from Thompson Coburn.

Last week, a California State Court became the first in the nation to rule that a retailer violated the Americans with Disabilities Act due to a website that is not accessible to individuals with vision-related disabilities.

The Federal Risk and Authorization Management Program, or FedRAMP, is a government-wide program to assess, monitor, and pre-authorize cloud-based products and services.

Recently revised cybersecurity regulations affecting US defense contractors and their subcontractors seek to address gaps in government contractor supply chains and expand the breadth of regulations in this area.

Explore critical insights on procurement fraud, clinical trials reform, cybersecurity threats, and leadership consensus. Discover how hidden relationships in procurement create financial risks, how Operation TrialBlazer aims to transform clinical trials, and why leadership teams must achieve consensus to drive execution and innovation.

Oh, the irony. Our federal government is filing lawsuits against private businesses and universities for having allegedly inaccessible websites and mobile apps when its own agencies have inaccessible websites.

My good friend Judy Greenwald at BusinessInsurance.com reported that Aon PLC stated that "Policyholders can expect 20% to 50% rate..

Cyber liability insurance policies vary widely, with dramatic difference in coverage.

Cyber coverage may be the hottest topic in the insurance industry. More carriers are offering cyber coverage, and more consumers are coming to the market, trying to figure out what to buy with their premium dollars.