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BioWorld - Friday, December 26, 2025
Home » Topics » Regulatory, BioWorld MedTech

Regulatory, BioWorld MedTech
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Bitcoin surrounded by coins and financial charts, symbolizing cryptocurrency and digital investment

Biopharmas launch new crypto financing strategies

Aug. 7, 2025
By Karen Carey
No Comments
With half-year industry financings down 59% from last year, and a U.S. administration supportive of cryptocurrencies, biopharma companies are building treasuries of digital assets to secure future R&D efforts and operational runways. Companies such as Artelo Biosciences Inc., MEI Pharma Inc., Windtree Therapeutics Inc. and 180 Life Sciences Corp. and have entered crypto deals in recent weeks, with the latter noting the potential to “unlock value outside traditional biotech milestones.”
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Laptop displaying FDA logo

FDA defends use of PFAS in medical devices

Aug. 6, 2025
By Mark McCarty
The U.S. FDA has staked out a position on the use of per- and polyfluoroalkyl substances in medical devices, declaring that the evidence offers no reason to restrict their continued use in med-tech products.
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Medicare puzzle

TEAM proposal beefed up in Medicare inpatient final for FY 2026

Aug. 5, 2025
By Mark McCarty
The U.S. Centers for Medicare & Medicaid Services adopted several significant policy changes in the Medicare inpatient final rule for fiscal 2026, which includes a larger rate bump for hospitals than seen in the draft.
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Hands holding arrow-shaped puzzle pieces

Olympus co-launches Swan as new JV for endoluminal GI robotics

Aug. 5, 2025
By Marian (YoonJee) Chu
Olympus Corp.’s “active investment” in endoluminal robotics has materialized in a new joint venture med-tech called Swan Endosurgical Inc., with Revival Healthcare Capital LLC.
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3D illustration of knee joint

NICE says multidisciplinary team needed for knee cartilage patient selection

Aug. 5, 2025
By Mark McCarty
The U.K. National Institute for Health and Care Excellence updated its guidance for the use of single-procedure insertion of scaffolds for knee cartilage repairs, specifying that only qualified surgeons should perform the procedure.
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Dollar sign between hands

FDA, industry gird for battle over next device user fee deal

Aug. 4, 2025
By Mark McCarty
Negotiations for the sixth U.S. FDA device user fee agreement (MDUFA VI) are officially underway, and the Aug. 4 meeting highlighted some of the differences between the agency’s and industry’s expectations.
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Product recall concept image

Dexcom recall triggered by reports of speaker malfunctions

Aug. 4, 2025
By Mark McCarty
The FDA announced July 17 that Dexcom Inc. recalled a series of continuous glucose monitor receivers for a failure of speakers to issue an alert for out-of-specification blood glucose measures. This is a clear demonstration of the principle that greater device functionality often creates new types of risk.
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Blue dollar sign on white background

Workload reductions figure into FDA’s FY2026 user fees

Aug. 4, 2025
By Mari Serebrov
No Comments
While inflation in the U.S. is hovering below 3%, increases in some FDA user fees for fiscal 2026 are tripling that rate. PDUFA fees for branded prescription drugs and biological products will see a 9% hike come Oct. 1, and the increase in MDUFA fees will more than double the inflation rate with a 7% hike across the board.
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Cybersecurity data lock

Illumina hit with $9.8M fine for unsecure sequencing equipment

Aug. 1, 2025
By Mark McCarty
The U.S. Department of Justice announced July 31 that Illumina Inc. agreed to pay $9.8 million to settle allegations it sold genomic sequencing equipment that suffered from cybersecurity problems. The settlement concludes a qui tam lawsuit filed by a former employee and highlights the hazards of poor cybersecurity for med-tech firms.
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Website of The Federal Trade Commission

US FTC snares $14.6M grant for technology upgrades

July 30, 2025
By Mark McCarty
The U.S. Federal Trade Commission announced a $14.6 million grant it received for an upgrade of its IT infrastructure. The same grant mechanism is leveraged by the Department of Justice, which is a clear sign that U.S. enforcement will be more vigorously enabled by sophisticated analytics going forward.
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