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BioWorld - Monday, April 13, 2026
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Spinal cord

Abbott launches IonicRF Generator in the U.S. to help those with chronic pain

Nov. 10, 2020
By Liz Hollis
Abbott Laboratories has seen the launch of the IonicRF Generator, which delivers a nonsurgical, minimally invasive treatment for the management of pain in the nervous system. The generator is a radiofrequency (RF) ablation device that uses heat to target specific nerves and block pain signals from reaching the brain. The launch of Abbott's IonicRF Generator looks to help the estimated 50 million people in the U.S. currently living with chronic pain.
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Digital illustration of U.S., coronavirus

Biden transition team plans for COVID-19 fight

Nov. 9, 2020
By Mari Serebrov
Preparing for a Biden presidency in which COVID-19 will be a top priority, the Joe Biden-Kamala Harris transition team named a board of scientists and public health experts Nov. 9 to advise the team on how to respond to the surging pandemic in the U.S.
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Lab equipment for cell-free DNA testing

Common mutations produce false positives in liquid biopsies used to guide cancer treatment

Nov. 6, 2020
By Annette Boyle
The use of liquid biopsies, tests that look for variants in cell-free DNA (cfDNA) shed by tumors into blood plasma, could lead to misdiagnosis and inappropriate treatment in many cancers, according to University of Washington researchers. The tests misidentified a noncancer mutation that is particularly common in older people as a mutation used as a biomarker for PARP inhibitors indicated for use in prostate cancer, a study published in JAMA Oncology found, but the problem likely extends to other malignancies.
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Blocks with gears, lightbulb, target, magnifying glass

Zimmer Biomet beats consensus in Q3, withholds 2020 guidance

Nov. 6, 2020
By Meg Bryant
Zimmer Biomet Holdings Inc. fell in line with other orthopedic device companies that saw better than expected results for the 2020 third quarter. The company reported total revenue of $1.93 billion, up 1.1% from the same period in 2019.
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Hand holding FDA blocks

HHS general counsel: FDA’s argument regarding LDT regulation falls short on several points

Nov. 6, 2020
By Mark McCarty
The controversy over the U.S. FDA’s authority to regulate lab-developed tests (LDTs) took on a new set of considerations due to the COVID-19 pandemic. However, a June 22 memo by HHS General Counsel Robert Charrow pokes holes in the FDA’s argument on several fronts. Among these is the question of whether an LDT can be regulated by the FDA, given that a test is not usually offered for sale across state lines.
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Dollar sign, up arrow

BD shines in Q4 with life sciences growing more than 30%

Nov. 5, 2020
By Liz Hollis
Becton, Dickinson and Co. (BD) reported good news Thursday, as it saw quarterly revenues of $4.784 billion for its fourth fiscal quarter, an increase of 4.4% over the prior-year period. Of note, the company’s life sciences segment saw worldwide revenues of $1.488 billion, representing an increase of 31.2% over the prior-year period as reported, or 31.4% on a currency-neutral basis.
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Fed Circuit answers Hatch-Waxman infringement venue question

Nov. 5, 2020
By Mari Serebrov
The U.S. Court of Appeals for the Federal Circuit narrowed the landscape for filing Hatch-Waxman infringement suits against U.S.-based companies, as it answered yet another question raised by the Supreme Court’s unanimous decision in TC Heartland v. Kraft Foods, which dramatically changed venue parameters in 2017 for all patent infringement cases.
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Coronavirus and stock charts

Haemonetics Q2 revenue down 17.1%, as plasma faces COVID-19 headwinds

Nov. 4, 2020
By Meg Bryant
Haemonetics Corp. reported sales of $209.5 million for the second quarter of fiscal year 2021, down 17.1% from the same period the prior year. Plasma sales declined 32.4% year over year to $78.4 million in the face of continuing COVID-19 impacts on blood donor activity. As Jeffries analyst Anthony Petrone observed, “Trough is rear view but plasma headwinds still elevated” through the period ended Sept. 26, “though declines were lower than expected (actual -30%; JEF -28% cc).”
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U.S. flag and money

MedPAC, industry, wary of proposed Medicare redefinition of reasonable and necessary

Nov. 3, 2020
By Mark McCarty
As might be expected, device makers have a lot of nice things to say about a recent proposal by the U.S. Centers for Medicare & Medicaid Services (CMS) to automatically cover technologies designated as breakthrough devices by the FDA. However, two trade associations and the Medicare Payment Advisory Commission (MedPAC) all expressed serious misgivings about a proposal to define the term “reasonable and necessary” as possibly contingent on private payer coverage.
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U.S. Capitol building

U.S. health policies will reflect congressional changes

Nov. 3, 2020
By Mari Serebrov
To say a lot is riding on the Nov. 3 presidential and congressional election in the U.S. would be an understatement, as the outcome could impact drug pricing, patent reform, research spending and pandemic response and preparedness.
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