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BioWorld - Monday, January 12, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Dec. 15, 2022

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Physiq's products

Physiq provides cardiopulmonary insight from daily-wear sensor

The move away from in-clinic testing continues, with another company offering a convenient, at-home sensor that gathers critical health information without requiring any change on the part of the patient, which may provide even more accurate, real-world data on patient health than the tests they replace. Read More

Abiomed pushing along treatment of right heart failure with Impella RP devices

Damage to the left ventricle may be more common than damage to its cousin on the other side, but right heart failure is still a unique syndrome with its own specific needs. Chuck Simonton, the chief medical officer at Abiomed Inc., told BioWorld that both the company and the U.S. FDA are keen to remind cardiologists that early detection and treatment of right heart failure vastly improves outcomes, including a huge reduction in mortality in these desperately ill patients. Read More
Ovarian cancer

Inoviq study confirms utility of exosome-based ovarian cancer screening diagnostic

A feasibility study conducted by the University of Queensland (UQ) confirmed the utility of Inoviq Ltd.’s exosome-based ovarian cancer screening test for isolating extracellular vesicle (EV) biomarkers. The Ovarian Cancer 97 study (OC97) screened data from 97 plasma samples and identified significant differences between the EV biomarker content of ovarian cancer and healthy control samples. Read More

FDA reissues inspection interference guidance to include device manufacturing facilities

The U.S. FDA has had a long-standing guidance dealing with drug manufacturing facilities that delay or deny FDA investigators’ attempts to inspect a manufacturing facility, but that policy was exclusive of device manufacturing facilities up until passage of the FDA Reauthorization Act (FDARA) of 2017. FDARA’s expansion of the policy to include device manufacturing facilities has prompted a rewrite of an existing 2014 guidance. Read More
Coins and financial paperwork

US SEC closes regulatory gaps to protect against insider trading

Responding to concerns about corporate insider trading, especially among life sciences companies, the U.S. SEC unanimously adopted final rules Dec. 14 establishing a 90-day cooling-off period before trades can be made under 10b5-1 plans that provide a safe harbor to insider trading. Read More

Appointments and advancements for Dec. 15, 2022

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

Financings for Dec. 15, 2022

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

Other news to note for Dec. 15, 2022

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Cardiacare, Endonovo, Evoendo, Insightec, Lumiradx, Medtronic, Pixium Vision, Prosomnus, Ra Medical. Read More

Regulatory actions for Dec. 15, 2022

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Life Spine, Medcognetics, Miromatrix, Providence Medical Technology, Thermo Fisher Scientific. Read More

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