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BioWorld - Friday, February 13, 2026
Home » PhRMA

Articles Tagged with ''PhRMA''

U.S. Supreme Court

Device, drug makers weigh in on Janssen’s FCA case

July 25, 2025
By Mark McCarty
Janssen Pharmaceutical’s loss in a False Claims Act (FCA) case for the company’s HIV treatments resulted in judgments of roughly $1.6 billion – an outcome the company appealed to the Court of Appeals for the Third Circuit.
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Speech bubbles

MIWG blasts FDA’s ‘piecemeal’ approach to regulated speech

Oct. 25, 2024
By Mark McCarty
The Medical Information Working Group again took up a question regarding U.S. FDA-regulated speech, citing the agency’s new misinformation draft guidance as an example of a piecemeal approach to regulated speech.
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Pills, bottle atop $100 bill

PhRMA challenge to US price negotiations lives again

Sep. 23, 2024
By Mari Serebrov
The U.S. Court of Appeals for the Fifth Circuit revived the Pharmaceutical Research and Manufacturers of America’s (PhRMA) constitutional challenge to the Medicare price negotiations, sending it back to a federal court in Texas for a do-over.
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Doctor and patient consultation

Patient perspective: Cost of Medicare negotiations not in dollars

Aug. 20, 2024
By Mari Serebrov
While the Biden administration continues applauding the savings it claims will be delivered by the first round of Medicare negotiations, many U.S. patients and their families are worried about the cost of the biopharma price-setting program – a cost they measure not in dollars and cents, but in worsening illness and lives that may be lost to a downturn in innovation and an upturn in barriers to access.
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Gavel and FTC logo

Trade associations push back on US PTO’s terminal disclaimer proposal

Aug. 1, 2024
By Mark McCarty
The proposal to overhaul the use of terminal disclaimers in U.S. patent filings won over no fans among former directors of the U.S. Patent and Trademark Office, but device and drug makers, too, are concerned about the proposal.
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Gavel and FTC logo

Trade associations push back on US PTO’s terminal disclaimer proposal

July 31, 2024
By Mark McCarty
The proposal to overhaul the use of terminal disclaimers in U.S. patent filings won over no fans among former directors of the U.S. Patent and Trademark Office, but device and drug makers, too, are concerned about the proposal.
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Revised 340B dispute resolution process ‘panders’ to hospitals

April 19, 2024
By Karen Carey
The Pharmaceutical Research and Manufacturers of America (PhRMA) is not happy with the Biden administration or the new 340B rule, finalized on April 18 by the U.S. Department of Health and Human Services (HHS), concerning the dispute resolution process put in place in 2020.
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US appeals court: States can fill the silence on 340B discounts

March 18, 2024
By Mari Serebrov
The U.S. Court of Appeals for the Third Circuit may have ruled last year that the Department of Health and Human Services doesn’t get to fill in the gaps in the law that created the 340B prescription drug discount program, but some states and lawmakers are coming up with their own workarounds to force drug manufacturers to give the discounts to an unlimited number of contract pharmacies.
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HHS scores first win in challenges to US price negotiations

Feb. 13, 2024
By Mari Serebrov
One down, eight to go. That’s the scorecard for the constitutional challenges to mandatory Medicare drug price negotiations now that a U.S. federal court has dismissed a suit filed by the Pharmaceutical Research and Manufacturers of America, the National Infusion Center Association and the Global Colon Cancer Association.
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US FDA importation approval: Worth the wait?

Jan. 8, 2024
By Mari Serebrov
With its approval Jan. 5 of Florida’s drug importation program, the U.S. FDA ended a 23-year wait for the government to implement a 2000 provision allowing certain prescription drug imports from Canada.
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