Natalia Mazina

AUGUST 16, 2022

Recently – on July 6, 2022 – the FDA amended the Emergency Use Authorization (EUA) for Paxlovid, an orally-administered COVID-19 therapeutic drug. Recently – on July 6, 2022 – the FDA amended the Emergency Use Authorization (EUA) for Paxlovid, an orally-administered COVID-19 therapeutic drug.

COVID-19 98

COVID-19 Informed Consent FDA Licensing 98

Healthcare IT News - Telehealth

MAY 24, 2021

In March 2020, the number of new COVID-19 infections was rapidly increasing in Washington. With no vaccination or specific treatment on the horizon, Howard University Hospital, an academic medical center in the district, prepared for a major surge of COVID-19 patients. Multi-way communication.

Patient Satisfaction 161

Patient Satisfaction Telemedicine Hospitals COVID-19 161

AIHC

SEPTEMBER 5, 2023

Compliance Considerations for Best Outcomes Written in collaboration with the AIHC Volunteer Education Committee Delivering mental health services via telehealth has increased since the COVID-19 pandemic. Higher rates of use of telehealth are now standard in many practices since the coronavirus disease 2019 (COVID-19) pandemic.

COVID-19 59

COVID-19 Telemedicine Compliance Informed Consent 59

Verisys

JANUARY 27, 2022

COVID has impacted every aspect of daily life, and these changes have affected people’s mental health, making telehealth services for behavioral health more important than ever. These license verification requirements have continued to change, so keeping up with regulations in telehealth is vital to compliance. According to the U.S.

US Department of Health and Human Services 52

US Department of Health and Human Services Telemedicine Licensing Informed Consent 52

SQA

FEBRUARY 15, 2023

Until EUDAMED is brought fully online, a series of performance study application/notification documents have been created to support performance study procedures with respect to the IVDR (see MDCG 2022-19). Decentralization is enabled by the advancement of digital tools, telemedicine, and more mobile and local healthcare.

US Department of Health and Human Services 40

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

Hall Render

FEBRUARY 10, 2023

billion since pandemic U.S. leading cause of death is heart disease, Alabama’s matches that Alabama lawmakers put temporary hold on $1 billion contract for prison healthcare New rolling NICU a ‘game changer’ for critical babies in Alabama More than a dozen Alabama hospitals at immediate risk of closing; officials say hospitals suffer $1.5

US Department of Health and Human Services 40

US Department of Health and Human Services COVID-19 Nursing Homes Nurses 40

Drug & Device Law

DECEMBER 29, 2023

Plaintiff knew about it, too, since he signed an informed consent document mentioning it. Equally bad, Hrymoc effectively read a New Jersey statute, §2A:58C-5(c), which precludes punitive damages where a “device” was “licensed” by the FDA, out of existence. The device labeling specifically mentioned it. The plaintiff in M.T.

FDA 105

FDA US Department of Health and Human Services COVID-19 Informed Consent 105