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Federal Judge Tells FDA it Must Make Public 55,000 Pages a

WEBA federal judge in Texas has ruled that the FDA must by the end of this month make public 12,000 pages of the data it used to make decisions about approvals for …

Actived: 6 days ago

URL: https://www.fdanews.com/articles/206113-federal-judge-tells-fda-it-must-make-public-55000-pages-a-month-of-pfizer-vaccine-data

FDA Collaborates with HealthVerity to Evaluate Real-World Data

WEBThe FDA has signed a multiyear agreement with Pennsylvania-based HealthVerity to evaluate real-world data to support the agency’s response to COVID-19. …

Category: Health Go Health

Diabetes Diagnosis and Management Could be Improved With …

WEBMarch 7, 2024. Digital health technologies are uniquely effective tools for screening, diagnosing, and managing both type 1 and type 2 diabetes, according to stakeholders …

Category: Health Go Health

FDA Grants EUA To iHealth's COVID-19 Self-Test Kit

WEBNovember 12, 2021. iHealth Labs has received the FDA’s Emergency Use Authorization (EUA) for over-the-counter sale of its COVID-19 Antigen Rapid Test. iHealth’s current …

Category: Health Go Health

Renewal of Public Health Emergency Means FDA’s Pandemic …

WEBIt’s official: The public health emergency (PHE) that is COVID-19 will continue for at least three more months. The Department of Health and Human Services …

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FDA Launches Next Gen Home Healthcare Device Development …

WEBFDA Launches Next Gen Home Healthcare Device Development Program. April 26, 2024. With an aim of supporting patients, medical device developers and …

Category: Medical Go Health

Global Medicine Spending and Usage Trends

WEB2 | Global Medicine Spending and Usage Trends: Outlook to 2025 Executive summary The COVID-19 pandemic has been the most impactful global health crisis in decades and …

Category: Medicine Go Health

FDA Seeks Comments on Greater Access to Medical Technologies …

WEBJune 6, 2023. As part of the FDA’s effort to increase access to home-use medical devices, CDRH is seeking comments from devicemakers, researchers, clinicians and the public …

Category: Medical Go Health

The US Active Pharmaceutical Ingredient Infrastructure: The

WEBThe US Active Pharmaceutical Ingredient Infrastructure: The current state and considerations to increase US Healthcare Security “Keeping the Nation’s drug …

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Managing Medical Device Recalls

WEBRecall Regulatory Framework. 21 C.F.R. Part 7 Subpart C is guidance, not law. Recalls conducted pursuant to Part 7 are “voluntary.”. Defines key terms and provides guidance …

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Patient-Focused Drug Development: Methods to Identify …

WEB94 Qualitative research methods (e.g., through interviews or focus groups), quantitative research. 95 methods (e.g., through survey instruments), or mixed-methods …

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CDRH Releases Guidances Intended for 2023 2022-10-18

WEBThe Center for Devices and Radiologic Health (CDRH) Monday released a priorities list of draft and final guidance documents it plans to publish in 2023, including …

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Health Canada Issues Guidance on Off-Label Uses of Drugs in

WEBHealth Canada released new guidance that the agency hopes will make it easier to study the off-label benefits of drugs in clinical trials. Canadian regulations …

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Corza Health to Merge with Surgical Specialties

WEBCorza Health has announced that it has merged with Surgical Specialties, a surgical-suture and ophthalmic-knife developer, to create a new surgical technology …

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Biosimilars in the United States 2020–2024

WEBiqviainstitute.org | 3 • In 2019, the United States spent $493 billion on medicines at ex-manufacturer invoice prices, including $211 billion on biologics, which now comprise …

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Big Health’s Sleepio App for Insomnia Gains NICE Recommendation

WEBThe U.K. National Institute for Health and Care Excellence (NICE) is recommending Big Health’s Sleepio software application for treatment for insomnia, for …

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POLICY ON REMAINING SHELF LIFE OF MEDICAL PRODUCTS

WEBWorking document QAS/19.788 Page 5 109 This document presents policy on shelf life and does not address details contained in other 110 guidelines, guides and agreements …

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other Tools) Resource BEST (Biomarkers, EndpointS, and

WEBBEST (Biomarkers, EndpointS, and other Tools) Resource [Internet]. Silver Spring (MD): Food and Drug Administration (US); 2016-. Co-published by National …

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