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BioWorld - Wednesday, April 15, 2026
Home » Topics » North America » U.S.

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Glass vial production line

GAO: Manufacturing the big challenge for COVID-19 vaccines

Feb. 11, 2021
By Mari Serebrov
Limited manufacturing capacity, supply chain disruptions and a dearth of personnel with specialized skills are all challenges vaccine makers are facing as they race to produce contracted quotas of COVID-19 vaccines that were developed and authorized in record time.
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DNA on digital background

NIH says phased genome assembly will enable preventive medicine

Feb. 10, 2021
By Mark McCarty
Preventive medicine hasn’t always had the backing of hard data, but research into genomics at the U.S. National Institutes of Health may soon change that.
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Bamlanivimab and etesevimab

FDA grants EUA for Abcellera-Junshi-Lilly COVID-19 treatment

Feb. 10, 2021
By Lee Landenberger
Another monoclonal antibody therapy has entered the pandemic fray with the FDA granting emergency use authorization (EUA) for bamlanivimab (LY-CoV555) 700 mg and etesevimab (JS016 or LY-CoV016) 1,400 mg as a cocktail for treating mild to moderate COVID-19 in patients aged 12 and up at high risk for progressing to severe COVID-19 and/or hospitalization.
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Generic drugs and bottle

Savings from complex generics remain elusive in U.S.

Feb. 10, 2021
By Mari Serebrov
Among the low-hanging fruit for pruning back U.S. drug prices is the development of generics referencing complex drugs, a category that includes drug-device combination products and nonbiologic drugs with a complex molecular base, route of administration or formulation, such as abuse-deterrent opioids.
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DNA on digital background

NIH says phased genome assembly will enable preventive medicine

Feb. 9, 2021
By Mark McCarty
Preventive medicine hasn’t always had the backing of hard data, but research into genomics at the U.S. National Institutes of Health may soon change that. Evan Eichler of the Howard Hughes Medical Institute said on a recent NIH webinar that phased genome assembly may allow medical science to efficiently treat diseases caused by genetic disorders, but will also enable preventive medicine, the holy grail of those who seek to restrain the ever-increasing cost of medical care.
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U.S. White House

White House vows to invoke DPA to respond to pandemic, including more at-home tests

Feb. 8, 2021
By Mark McCarty
The Biden administration said it will use the U.S. Defense Production Act to grapple with the COVID-19 pandemic in a plan that includes a large increase in vaccine purchases. Also on tap is an increase in production of at-home test by six companies in addition to Ellume Ltd., of Perth, Australia, which will ship more than 8 million of their tests to the U.S. by the end of the year.
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Two arrows in opposite directions

Zimmer Biomet streamlines focus with spinoff of spine and dental businesses

Feb. 8, 2021
By Meg Bryant
Zimmer Biomet Holdings Inc. continued its transformation, disclosing Friday that it will spin off its spine and dental businesses into a separate, publicly traded company. The move will enable the independent company, identified as Newco, to pursue strategies and growth in spine and dental solutions that have not been a major focus for Zimmer Biomet, while allowing the latter to focus on high-growth orthopedic segments.
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Illustration of head, brain blood flow with Novaguide

Novasignal launches app to rapidly communicate cerebral ultrasound data

Feb. 5, 2021
By Mary Ellen Schneider
Novasignal Corp. has a launched a cloud-based app to provide alerts to clinicians directly from its cerebral ultrasound device. The new app allows physicians to get instant notifications from the company’s Novaguide device, a transcranial doppler ultrasound technology that allows for real-time assessment of blood flow in the brain by combining robotics and artificial intelligence (AI).
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FDA icons

Regulatory attorney says warning letters likely to spike under new FDA administration

Feb. 4, 2021
By Mark McCarty
U.S. FDA warning letters have been a staple of regulatory life since the late 1990s, but James Boiani, a regulatory attorney with Epstein, Becker & Green P.C., said it’s no stretch of the imagination that warning letter volumes will jump in 2021. This is to some extent because the volume of warning letters dropped significantly over the past four years, and Boiani advised that all FDA-regulated industries will see more warning letters unless they are communicative with the agency about inspectional findings.
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Blocks with upward arrows

BD posts strong Q1 results for 2021

Feb. 4, 2021
By Meg Bryant
Becton, Dickinson and Co. (BD) reported revenue of $4.32 billion for the first quarter of fiscal year 2021, up 25.8% on a reported basis and 24.3% on a currency neutral basis. COVID-19 testing contributed 20.5% of that growth, totaling $867 million for the period, including $688 million in Veritor Plus system sales.
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