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BioWorld - Monday, March 30, 2026
Home » Topics » Regulatory » NIH

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Regulatory front for Dec. 28, 2020

Dec. 28, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: CMS unveils push toward digital collection of quality measures; NIH awards for ‘outside-the-box’ projects under RADx; ISO posts IP management standard.
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U.S. Capitol and $100 bills

Congress gives NIH, FDA slight funding bump for fiscal 2021

Dec. 22, 2020
By Mari Serebrov
After nearly three months of the U.S. federal government operating on stopgap spending measures, Congress has agreed to a $1.4 trillion spending bill for fiscal 2021. The omnibus package, which includes $97 billion for the Department of Health and Human Services, gives both the FDA and NIH small increases in funding.
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NIH trial testing Lilly antibody against COVID-19 paused

Oct. 13, 2020
By Michael Fitzhugh
An NIH-sponsored phase III trial testing Eli Lilly and Co.'s SARS-CoV-2 neutralizing antibody candidate, LY-CoV555, alongside the Gilead Sciences Inc. antiviral Veklury (remdesivir) has been paused at the request of its data safety monitoring board, the company told BioWorld.
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Diagram explaining COVID-19 Decompensation Index workflow

Physiq begins development of AI-based COVID-19 early warning system

Sep. 21, 2020
By Mary Ellen Schneider
The digital medicine company Physiq Inc. has received a contract from the NIH to develop an artificial intelligence (AI)-based index that can provide an early warning that a patient with COVID-19 is in decline and needs medical treatment. The index, called the COVID-19 Decompensation Index (CDI) Digital Biomarker, will run on Physiq’s existing Accelerateiq computing platform, analyzing physiological data from FDA-cleared wearable devices to create a personalized baseline for patients who have tested positive for COVID-19.
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Plasma bag

Dueling plasma guidelines a sign of the times

Sep. 3, 2020
By Mari Serebrov
While the emergency use authorization (EUA) the FDA granted Aug. 23 for convalescent plasma remains a political talking point, the agency moved ahead Sept. 2, issuing an updated, immediately effective guidance on the use of convalescent plasma to treat COVID-19 patients in ongoing clinical trials, on an expanded access basis or under the EUA.
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U.S. NIAID Director Anthony Fauci

Fauci ‘cautiously optimistic’ about a vaccine for COVID-19, says scientific values not compromised

July 31, 2020
By Mark McCarty
The issue of the U.S. federal government’s response to the COVID-19 pandemic was revisited yet again in a hearing in the House of Representatives. While partisanship was on full display, Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, said he is “cautiously optimistic” about the prospects for a vaccine and that the development of candidates has not compromised scientific principles.
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ENCODE project illustration
Phase IV now underway

Data reported from ENCODE phase III

July 29, 2020
By Anette Breindl
Researchers from the Encyclopedia of DNA Elements (ENCODE) consortium reported data from the third phase of the project. Phase III data, which were published in more than a dozen papers in Nature and its sister journals on July 29, 2020, consisted of 6,000 experiments performed on around 1,300 samples.
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U.S. flag and money

Partisan votes on U.S. federal agency appropriations foreshadow showdown between House, Senate

July 8, 2020
By Mark McCarty
Two subcommittees of the U.S. House Appropriations Committee have moved their respective appropriations proposals for the FDA and the NIH, restarting a process that has worked smoothly over the past couple of years. Still, Republicans in both committees objected to the use of emergency funding mechanisms in lieu of more routine appropriations.
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Coronavirus vaccine/therapeutics illustration

Taxpayer-enabled COVID-19 vaccines will cost less, but distribution system requires another at-risk investment

July 2, 2020
By Mark McCarty
The question of prices for a COVID-19 vaccine have raged in recent days. Gary Disbrow, acting director of the Biomedical Advanced Research and Development Authority (BARDA), told members of a Senate committee that vaccines developed with the help of taxpayer funding will come with an appropriate reduction in price. However, CDC Director Robert Redfield emphasized that the cold-chain distribution system for those products requires the same kind of at-risk investment that is used for vaccine development.
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Coronavirus vs U.S. wrecking balls

Pandemic-weary nation prepares for next COVID-19 wave

June 23, 2020
By Mari Serebrov
The bad news is, yes, the U.S. is in for a second wave of COVID-19, which is expected to hit during the upcoming flu season. The good news is the nation is much better prepared for the next wave, the NIH’s Anthony Fauci told a House Energy and Commerce Committee Tuesday.
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