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BioWorld - Tuesday, December 16, 2025
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

May 29, 2024

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Camaps FX closed loop system

FDA approves first algorithm for use in pregnant women with type 1 diabetes

The U.S FDA approved Camaps FX for use in pregnant women with type 1 diabetes. This first, hybrid, closed-loop app was developed by Camdiab Ltd., a spinout from Cambridge University, allows individuals aged two years and older with type 1 diabetes to manage their glucose levels. Read More
FDA-yellow-dice.png

Industry wary of limitations on FDA’s pre-submission program

The U.S. FDA’s reissued draft guidance for pre-submission activity addresses the circumstances in which a manufacturer’s questions can be handled informally, but industry has a few misgivings about the draft. One of these is that a preformatted template proposed by the FDA would limit the number of topics that can be handled in an informal manner, which the Advanced Medical Technology Association said might drive more utilization of formal pre-submission programs, an outcome that would thwart the intent of these informal interactions. Read More
Map of Europe, Medical Device Regulation (MDR) text

Team NB sees widening gap between MDR applications, certificates

The European Association for Medical Devices of Notified Bodies has issued its survey of member NBs for 2023, which includes data that suggest a diminishing appetite for inspections under the Medical Device Single Audit Program. However, the more concerning metric is that the gap between applications for new or renewed medical devices and the number of completed applications continues to widen, a gap that stood at nearly 10,000 such applications at the end of calendar year 2023. Read More

US NIH step closer to including price, as access, in licenses

Price is working its way indirectly into licensing agreements for U.S. NIH-funded inventions, be they drugs, biologics, vaccines or medical devices. Read More
Judge's gavel with US flag

ACLA files suit against US FDA over lab-developed test final rule

The American Clinical Laboratory Association has followed through on its promise to file suit against the U.S. FDA over the agency’s final rule for lab-developed tests. The lawsuit will be heard in the U.S. District Court for the Eastern District of Texas, which is also the venue for litigation against another federal government agency, the Federal Trade Commission, suggesting that litigants expect a favorable review of their case in this court. Read More
belle ai skin

Belle.ai patents AI platform for evaluating, tracking skin conditions

A little over two months after the granting of its very first patent which described computer-based systems for diagnosing psoriasis, Belletorus Corp. welcomed the publication of two continuation-in-part child filings on similar such systems for the diagnosis of eczema and determining the severity of skin diseases such as psoriasis, eczema and skin cancer. Read More

Appointments and advancements for May 29, 2024

New hires and promotions in the med-tech industry, including: Augmedix, Delcath. Read More

Financings for May 29, 2024

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

In the clinic for May 29, 2024

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Baxter, Kardium, Octave Bioscience. Read More

Other news to note for May 29, 2024

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Canary Medical, Cancer Check Labs, Mannkind, Pulmatrix, Surmodics. Read More

Regulatory actions for May 29, 2024

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Beckman Coulter, Vuze Medical. Read More

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