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BioWorld - Thursday, January 15, 2026
Home » Topics » Regulatory

Regulatory
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U.S. Capitol building
FDLI Advertising and Promotion Conference

US data privacy environment a tangled web for med-tech companies

Nov. 3, 2023
By Mark McCarty
Privacy considerations have been front and center for U.S. federal government agencies for more than two decades, but several states have jumped into the privacy arena with their own legislative imperatives. While companies in the medical device industry would like to see a less imposing thicket of related enforcement requirements, Nancy Perkins of Arnold & Porter LLP said there is little prospect that Congress will relieve the predicament with anything resembles preemptive legislation.
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Regulatory actions for Nov. 3, 2023

Nov. 3, 2023
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbott, Empatica, Polaris.
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Immuno-oncology

Prokarium’s ZH-9 cleared to enter clinic in US for bladder cancer

Nov. 3, 2023
Prokarium Ltd. has obtained FDA clearance of its IND application for ZH-9 for patients with non-muscle invasive bladder cancer.
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Antibody-drug conjugate
Immuno-oncology

Angiex cleared to begin phase I study of TM4SF1-directed ADC

Nov. 3, 2023
Angiex Inc. has received FDA clearance of its IND application for AGX-101, a novel TM4SF1-directed antibody-drug conjugate (ADC) being developed for the treatment of solid cancers.
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Dollar sign inside vial, syringe

Interchangeable to challenge Stelara, impact of price negotiations still a question

Nov. 2, 2023
By Mari Serebrov
Instead of the two-step process that’s been the typical path for interchangeables in the U.S., Amgen Inc.’s Wezlana got a green light Oct. 31 from the FDA as both the first approved biosimilar and interchangeable to Johnson & Johnson’s inflammatory disease drug, Stelara (ustekinumab).
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Voquezna

Voquezna GERD approval in hand, Phathom set to launch by year-end

Nov. 2, 2023
By Randy Osborne
Phathom Pharmaceuticals Inc. will begin marketing Voquezna (vonoprazan) in December, thanks to the Nov. 1 approval by U.S. regulators, who cleared the potassium-competitive acid blocker at 10-mg and 20-mg doses for all grades of erosive gastroesophageal reflux disease (GERD), maintenance of healing of all grades of the condition and relief of associated heartburn.
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OMB memo on AI suggests need for more IT capacity at US FDA

Nov. 2, 2023
By Mark McCarty
As a follow-up to the Biden administration’s executive order for artificial intelligence (AI), the U.S. Office of Management and Budget (OMB) has promulgated a memorandum directing federal government agency use of AI.
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Laptop displaying FDA logo
FDLI Advertising and Promotion Conference

US DOJ: company history, potential for harm drive criminal charges for marketing

Nov. 2, 2023
By Mark McCarty
The U.S. Department of Justice (DOJ) has a unique role in enforcement of medical product communication even though the department shares oversight of medical product promotions with the FDA and the Federal Trade Commission (FTC).
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sibionics cgm

Sibionics lands CE mark for GS1 CGM system

Nov. 2, 2023
By Marian (YoonJee) Chu
Sibionics Technology Co. Ltd. said it received the CE mark for its continuous glucose monitoring (CGM) system, coined the Sibionics GS1 CGM, helping the company expand its market opportunities beyond China.
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Regulatory actions for Nov. 2, 2023

Nov. 2, 2023
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Toku.
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