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BioWorld - Tuesday, April 28, 2026
Home » Topics » Regulatory

Regulatory
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Decorative scales of justice in a courtroom

Texas AG claims Eli Lilly assistance programs a bribe

Aug. 13, 2025
By Mari Serebrov
No Comments
Doing his version of the Texas Two-Step, Texas Attorney General (AG) Ken Paxton is again shuffling Eli Lilly and Co. into a state courtroom – this time for allegedly overstepping the anti-kickback line.
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Hands holding arrow-shaped puzzle pieces

Deephealth closes $110M Icad buy, gains Techlive clearance

Aug. 12, 2025
By Annette Boyle
Deephealth Inc., a subsidiary of Radnet Inc., completed the acquisition of breast health solutions company Icad Inc. in a $110 million all-stock transaction. The company also received U.S. FDA 510(k) clearance for Techlive – a remote scanning solution enabling centralized operation and supervision of MR, CT, PET/CT and ultrasound procedures.
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Nyxoah Genio

Nyxoah wins FDA approval for Genio OSA treatment

Aug. 12, 2025
By Holland Johnson
Nyxoah SA may now help make dreams come true here in the U.S. with its FDA approval for the Genio system for the treatment of obstructive sleep apnea.
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U.K. flag on stethoscope

TEAM NB proposes centralized resource office to deal with MDR, IVDR

Aug. 12, 2025
By Mark McCarty
The issues facing the EU’s Medical Device Regulation and the In Vitro Diagnostic Regulation are the stuff of legend, but the EU’s notified body group, TEAM NB, has proposed a mechanism to deal with some of the administrative problems.
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Whoop band

FDA warning raises Whoop's blood pressure

Aug. 12, 2025
By Mark McCarty
The FDA’s warning letter to Whoop Inc. resurrects questions about the agency’s observance of the 21st Century Cures Act in that the warning letter stakes out the position that any reading of blood pressure is “inherently associated” with hypertension.
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Bone marrow illustration with doctor background

Syntara’s stock plunges 52% following FDA request for added trial

Aug. 12, 2025
By Tamra Sami
No Comments
Syntara Ltd.’s stock plummeted 52% on news that the FDA recommended an additional phase IIb trial following a type C meeting about the company’s clinical development plan for lysyl oxidase inhibitor amsulostat (SNT-5505, formerly PXS-5505) in myelofibrosis.
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COVID-19 mRNA vaccine vials, syringe

KDCA readies mRNA vaccines, tech for COVID-19, future outbreaks

Aug. 12, 2025
By Marian (YoonJee) Chu
No Comments
Korea Disease Control and Prevention Agency (KDCA) secured 5.3 million doses of COVID-19 vaccines made by Pfizer Inc./Biontech SE and Moderna Inc., officially including the mRNA-based vaccines in the country’s national immunization program on Aug. 5.
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Setpoint vagus nerve stimulation device

Setpoint sports back-to-back wins with FDA approval, $140M raise

Aug. 11, 2025
By Annette Boyle
In less than two weeks, Setpoint Medical Inc. mastered the power serve with the first approval of a neuroimmune modulation device to manage rheumatoid arthritis, followed by a $25 million second tranche of its series C and a $115 million series D financing round.
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U.S. FDA headquarters

Industry sees need for clarity in FDA draft guidance for 510(k) transfers

Aug. 11, 2025
By Mark McCarty
Eleven pages is relatively short for a modern U.S. FDA draft guidance, but two trade associations nonetheless had questions about the FDA draft for transfers of 510(k) devices, such as how the agency defines the holder of the 510(k).
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US flag, gavel, book

Spinefrontiers CEO sentenced to one year of supervised release

Aug. 11, 2025
By Mark McCarty
Kingsley Chin, the CEO of Spinefrontier Inc., has been sentenced to a year of supervised release for his role in the payment of less than $5,000 in consulting fees to a surgeon who provided no consulting services.
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