MedCity News

MedCity News

MedCityNews is a top online platform that covers the business side of healthcare innovation. We provide valuable insights into upcoming trends and important topics through a combination of breaking news and in-depth analysis. Our content focuses on both emerging startups and well-known industry figures, as well as key policies and significant deals in the healthcare sector.

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  • 1 day ago | medcitynews.com | Travis Bias

    Two years ago, every health conference I attended had multiple panels on clinician burnout. The problem is well known, and the actual system-level contributors have been called out. In the last year, the solution to burnout is splashed on every conference app log-in screen: generative artificial intelligence (AI).

  • 1 week ago | medcitynews.com | Frank Vinluan

    A Gilead Sciences drug that protects against HIV infection has won a highly anticipated FDA approval, becoming the first medication for HIV prevention available as a twice-yearly injection. The regulatory decision announced Wednesday covers use of the antiviral drug, lenacapavir, for HIV-1 pre-exposure prophylaxis (PrEP). The approval is for adults and adolescents weighing at least 35 kg (about 77.1 pounds) who are at risk of sexually acquired HIV-1.

  • 1 week ago | medcitynews.com | Stephanie Baum

    Are you developing health tech solutions with AI? We’re looking for the next wave of digital health startups using artificial intelligence to transform the day-to-day work of providers. If your solution streamlines diagnosis, clinical documentation, scheduling, or patient engagement, we’d welcome your application to Pitch Perfect at INVEST Digital Health. The conference is scheduled for September 18 in Dallas, Texas at Pegasus Park, in collaboration with Health Wildcatters. To apply, click here.

  • 1 week ago | medcitynews.com | Frank Vinluan

    The FDA is implementing a new pilot program that could incentivize development of certain new drugs by dramatically shortening their regulatory reviews. But to qualify, a drug must address specified national health interests. The FDA already has a program that speeds up regulatory review of rare disease drugs. This priority review voucher program (PRV) was created by Congress, initially for rare and neglected diseases, then later expanded to include rare pediatric diseases.

  • 1 week ago | medcitynews.com | Marissa Plescia

    Employers are already struggling with rising healthcare costs in 2025, and early signs suggest these challenges will persist — potentially worsening in 2026, according to Tracy Watts, senior partner at consulting firm Mercer. And it’s getting to a point where employers may have to start shifting costs to employees, she added.