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 Are Hospitals Ready for Alzheimer’s Treatment Approval?

HIT Consultant

John Showalter, MD, Chief Product Officer at Linus Health The FDA’s recent accelerated approval of Leqembi was welcome news across the Alzheimer’s community. It is expected to be more than six times the size of the public health campaign for COVID-19. billion marketing the medication.

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5 Key Facts to Know About FDA’s Emergency Use Authorization Process

Exeed Regulatory Compliance

How Emergency Use Authorization of Medical Products Helps Provide Relief During a COVID-19 Major Crisis. The current COVID-19 global pandemic continues to remain out of control. It is a public health emergency of massive scale that has affected nearly all aspects of our life.

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Telehealth and RPM – 2023 Health IT Predictions

Healthcare IT Today

As we head into 2023, we wanted to kick off the new year with a series of 2023 Health IT predictions. Digitally-enabled care is the future of telehealth – “telehealth” has become industry norm since the start of the pandemic and used as a catchall term for everything from virtual doctor’s appointments to at-home testing kits.

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The Retail Health Battle Royale in the U.S. – A Week-Long Brainstorm, Day 3 of 5 – Apple as “Intelligent Health Guardian”

Jane Sarashon

Apple wants to be your “intelligent guardian for health,” based on a 60-page paper shepherded by Jeff Williams, the company’s Chief Operating Officer. I’m folding the report into my coverage this week on the Retail Health Battle Royale today, Day 3 of my week-long series updating us on the health/care ecosystem.

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How the Medical Industry Can Help Combat the Current Coronavirus Crisis

Exeed Regulatory Compliance

A novel coronavirus, now called SARS-CoV-19, was first detected in the Hubei province of China in early December 2019. Secretary of the Department of Health and Human Services (HHS) has declared a public health emergency. Global outbreak of the recent novel coronavirus needs an all-hands-on-deck approach.

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – January

SQA

Relevant matters are hereby announced as follows: As of 01 December 2022, the Electronic Certificates of Documentation for Export of APIs to the EU and Certificate of a Pharmaceutical Product will be put into use. Efforts should be made to promote and guide the use of electronic certificates.

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How to win physician confidence in remote patient monitoring programs

Healthcare IT News - Telehealth

Clinical Decision Support Electronic Health Records (EHR, EMR) Telehealth Workflow CIOs need to look beyond just EHRs and explore standalone platforms to enhance care delivery – keeping focused on reliable patient data and streamlined clinical workflows. For reimbursement by the CMS, a device must be an FDA-listed device.