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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

May 1, 2024

View Archived Issues
Regulatory-US-FDA-HQ.png

FDA wary of impact of retirements on inspectional activities

The U.S. FDA’s senior managers often lament the lack of routine increases in taxpayer funding, a concern that Michael Rogers, the associate FDA commissioner for regulatory affairs, reiterated during a May 1 webinar. Rogers said the agency’s field inspectorate will be working through a large number of retirements over the next few years, a predicament he said will continue to be “a huge challenge” to overcome. Read More
Tinted Euro symbol

Europe med-tech startups continue to struggle to raise funds

Despite a couple of med-tech deals transacted this year and more liquidity in the market, early-stage medical device companies in Europe continue to struggle to raise funds. To attract interest from Venture Capital (VC) funds, these companies must ensure they have a disruptive technology, be willing to change their story, and do the math to ensure that VC firms who back them can get an adequate return, investors advised at the recent LSX World Congress in London. Read More
Cardinal Health Monoject Disposable Syringes

US FDA drops warning on Cardinal Health over third party devices

The U.S. FDA issued a handful of warning letters to device makers in the month of April 2024, one of which is for the Waukegan, Il., plant operated by Cardinal Health Inc., of Dublin, Ohio. While the Waukegan plant escaped citations for most routine Quality System Regulation deviations, the FDA said Cardinal’s handling of contract manufactured luer locks and syringes fell well short of the agency’s expectations given that these issues led to a massive recall, a product removal and an FDA advisory. Read More
Illustration of brain with electrical activity background

Epitel snags FDA clearance for two epilepsy devices

Epitel Inc. received U.S. FDA clearances for two epilepsy-focused technologies that simplify detection and analysis of seizures in patients with suspected epilepsy. The Remi remote electroencephalogram monitoring system is a wearable device that allows patients to continue with their daily activities for extended periods without the restrictions of wires, while still capturing intermittent seizures. The Remi Vigilenz artificial intelligence system uses machine learning to identify and note seizure events in the Remi EEG records. Read More
Medtronic's Inceptiv neurostimulator

Medtronic wins FDA approval for pain-sensing spinal cord stimulator

Medtronic plc said it secured U.S. FDA approval for its first closed-loop spinal cord stimulator (SCS), designed to take in signals from the body and adjust its therapy automatically. Read More

Debate over Orange Book device listings heard on multiple fronts

Just a few days after the U.S. Congressional Research Service issued a report suggesting ways Congress could resolve the unanswered questions about patent listings in the FDA’s Orange Book, the FTC sent a second round of warning letters to eight biopharma companies and their subsidiaries, citing the listing of device patents for combination products. Read More

Appointments and advancements for May 1, 2024

New hires and promotions in the med-tech industry, including: Agilent, Arcuro, Biosig, Nymbl, Staar Surgical. Read More

Financings for May 1, 2024

Med-tech firms raising money in public or private financings, including: Trisalus. Read More

In the clinic for May 1, 2024

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Biocardia. Read More

Other news to note for May 1, 2024

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: GT Medical, Limbus AI, Magventure, Magnus Medical, Pavmed, Radformation, Retispec, Theragenics, Topcon Healthcare, Verantos, Veris. Read More

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