FDA Releases Guidelines on Regulation of Medical Software
The FDA has updated guidance on which medical devices are regulated by the agency.
FDA Issues Warning About Serious Security Flaws in Critical Medical Devices
The FDA warns manufacturers, healthcare providers, hospitals and patients that the “URGENT/11” security flaws may cause medical devices to malfunction.
Resolving Health IT-Related Patient Safety Events
Ensuring health information technology-related events are resolved and incorporate effective solutions should be a continued focus area for healthcare systems.
HHS Draft Strategy Addresses Clinical Burden of EHRs and Other HealthIT
ONC has released a draft strategy it believes will lessen the regulatory and administrative burden of health information technologies, such as EHRs. MLMIC encourages all insured stakeholders to take this opportunity to offer their input.