CMS.gov
APRIL 15, 2019
Ensuring Safety and Quality in America’s Nursing Homes. Nursing facilities. This duty is especially important when it comes to the care provided for some of the most vulnerable in our society, Americans residing in nursing homes. CMS’ approach to oversight of nursing homes is constantly evolving.
Med-Net Compliance
OCTOBER 6, 2022
An Iowa nursing home was cited for placing its residents in immediate jeopardy after a resident became wedged between a bed and a grab bar and suffocated. The post Iowa Nursing Home Resident Suffocated Due to Grab Bar Entrapment appeared first on Med-Net.
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Exeed Regulatory Compliance
MARCH 22, 2020
A new FDA guidance provides much-needed relief during a pandemic. FDA has just revised its relatively less known 2012 guidance entitled “Post-market Adverse Event Reporting for Medical Products and Dietary Supplements During an Influenza Pandemic” to clarify that the guidance is applicable to any pandemic, not just an influenza pandemic.
Healthcare IT News - Telehealth
MAY 6, 2020
It also equips providers with Eko’s FDA-cleared AI to assist in remote screening for AFib, heart murmurs, tachycardia and bradycardia. A provider present with the patient at one location – a nursing home, community clinic, etc. The system can be used to conduct telehealth visits between two or more clinics.
SQA
SEPTEMBER 2, 2022
United States Food and Drug Administration (FDA) – Regulations and Guidances. FDA Proposes Benefit-Risk Considerations for Product Quality Assessments, 20 June 2022. The FDA is announcing the availability of a draft guidance for industry entitled Conducting Remote Regulatory Assessments, Question and Answers.
Healthcare IT Today
JULY 30, 2023
One culprit is staffing in post-acute care – 87% of nursing homes report moderate to high staffing shortages. UltraSight was granted FDA clearance for its AI-powered ultrasound guidance technology. Nearly two-thirds (63%) of U.S.
SQA
MAY 17, 2022
United States Food and Drug Administration (FDA) – Regulations and Guidances. The FDA proposes to do so primarily by incorporating by reference the 2016 edition of the international standard specific for medical device quality management systems set by the International Organization for Standardization (ISO), ISO 13485.
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