Electronic Health Reporter

JULY 22, 2019

Health information management leaders told members of Congress today that removal of a nearly two-decade ban on the use of federal funds to adopt a nationwide unique patient identifier would allow collaboration between the U.S.

119

119

HIT Consultant

JULY 27, 2023

This includes nurse and clinician shortages, which persist across hospitals and health systems nationwide. When it comes to patient safety, nurses want to ensure that they’re providing the best possible care. One of the keys to addressing burnout is providing nurses with professional development opportunities.

Nurses 98

Nurses COVID-19 Hospitals Public Health 98

Healthcare IT Today

JANUARY 4, 2023

Healthcare organizations essentially need to clean out their IT garage and look for the solutions that tackle their most critical issues while offering streamlined compatibility and impacting patient care. Additionally, labor shortages will double the medication error rate among providers, according to Forrester.

Hospitals 104

Hospitals Health Outcomes Medical Billing Nurses 104

Healthcare IT Today

FEBRUARY 15, 2023

Efforts to identify the right path forward for healthcare’s patient matching problem are gaining a foothold as stakeholders from across the spectrum come together to remove obstacles and implement effective solutions. Why it Matters Patient misidentification issues cost the average healthcare facility $17.4

US Department of Health and Human Services 115

US Department of Health and Human Services COVID-19 Public Health Hospitals 115

SQA

OCTOBER 18, 2023

In view of these facts, the Federal Police were involved in the case, which resulted in the seizure of irregular finished products (specifically, medical drug without registration, with false labeling information) and raw materials (specifically, vegetable drugs) that were used in the manufacture of irregular products.

FDA 40

FDA Compliance Licensing World Health 40

SQA

DECEMBER 10, 2021

Brazil’s New UDI Requirements for Medical Devices: Compliance Implications for Manufacturers, 02 August 2021. ANVISA has rolled out its proposed framework for Unique Device Identification (UDI) requirements. China: National Medical Products Administration (NMPA).

FDA 52

FDA Compliance Public Health Hospitals 52

SQA

OCTOBER 18, 2022

The counterfeit devices were sold online by a distributor named Healthful Plus without the required license to import, distribute, or sell medical devices in Canada. device identifier “COV-19C25.” appears to no longer be manufacturing medical devices. These ingredients could interact with other medications and foods.

US Department of Health and Human Services 40

US Department of Health and Human Services FDA COVID-19 Compliance 40