Compliance FDA Nursing Homes 
Healthcare IT News - Telehealth
MAY 6, 2020
The company’s Carnation Ambulatory Monitor (CAM) Patch is a P-wave centric ambulatory cardiac monitor and arrhythmia detection device that also is designed to improve patient compliance for both adults and children through its lifestyle-enabling form factor. iRhythm Technologies.
MedTrainer
OCTOBER 27, 2020
Keys to managing point-of-care testing compliance. In an effort to combat the spread of the virus and to help nursing homes protect the health and safety of their residents, the U.S. To be eligible, nursing homes must have a current CLIA Certificate of Waiver and meet certain epidemiological criteria.
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MedTrainer
OCTOBER 27, 2020
Keys to managing Point-of-Care Testing Compliance. Keys to managing point-of-care testing complianceIn an effort to combat the spread of the virus and to help nursing homes protect the health and safety of their residents, the U.S.
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.
SQA
SEPTEMBER 2, 2022
ISPE Good Practice Guide: Critical Utilities GMP Compliance. United States Food and Drug Administration (FDA) – Regulations and Guidances. FDA Proposes Benefit-Risk Considerations for Product Quality Assessments, 20 June 2022. ISPE Good Practice Guide: Ozone Sanitization of Pharmaceutical Water Systems .
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.
SQA
MAY 17, 2022
China Regulatory Roundup: Latest Guidelines for Medical Device and IVD Compliance, 17 March 2022. United States Food and Drug Administration (FDA) – Regulations and Guidances. Guidance for Industry: Certain Ophthalmic Products: Policy Regarding Compliance with 21 CFR Part 4, March 2022.
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