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BioWorld - Monday, March 23, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Jan. 27, 2022

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Deadlines a sticking point in FDA’s Section 522 studies draft guidance

The U.S. FDA often has difficulty turning around draft guidances into final guidances in a timely manner, but that hasn’t impeded the agency’s appetite for fast turnaround of industry responses to FDA mandated postmarket surveillance studies. Nonetheless, the Medical Device Manufacturers Association (MDMA) said in comments to the docket for the May 2021 draft guidance for Section 522 postmarket surveillance studies that a requirement that such a study be fully enrolled within 24 months should be aspirational rather than compulsory. Read More
Team member headshots in a grid

Precision genomics startup Tensixteen Bio launches with $40M

Investors have backed a new precision medicine company targeting clonal hematopoiesis with $40 million. Tensixteen Bio Inc. is on a mission to understand how somatic mutations influence age-related diseases, including cancer. The San Francisco-based startup will use the funds to develop a genomics and clinical platform that can identify patients at high risk of developing disease. Read More
Gavel and stacks of coins

Australia’s TGA to increase industry fees to retain its cost recovery model

PERTH, Australia – Australia’s Therapeutic Good Administration (TGA) plans to increase all fees and charges to industry by 2.6% for the 2022 to 2023 financial year, and it is seeking feedback on proposed options. Read More
BD Max system in use

Clinicians miss 45% of vaginitis cases, BD says

Molecular diagnostics could dramatically improve care for one of the most common infections women face, vaginitis. A study by Becton, Dickinson and Co. (BD) found that clinicians miss more than 45% of positive cases and misidentify an additional 12% of negative cases as positives when compared to diagnostic findings. Read More
Eyelib in an eye clinic

Mikajaki reported European commercial launch for its automated ophthalmic diagnostics platform

PARIS – Mikajaki SA reported the commercial launch of Eyelib, a robotic ophthalmic diagnostics platform. One year after obtaining CE marking, the Swiss-based med-tech is rolling out a wide-scale launch of its automatic ophthalmology examination system onto the European market. Read More
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Med-tech industry sees persistent hazards in ongoing CPU shortage

The semiconductor industry has been hit hard by shortages of computer central processing units (CPUs) in recent months, but the persistence of these shortages has prompted a new response from industry. The Advanced Medical Technology Association (AdvaMed) said device makers are taking steps to ease the crunch, but that the Biden administration must take steps to ensure that medical technologies do not suffer from shortages, given the critical role played by devices in patient care. Read More

Appointments and advancements for Jan. 27, 2022

New hires and promotions in the med-tech industry, including: Intelligent Implants, Mainz Biomed. Read More

Financings for Jan. 27, 2022

Med-tech firms raising money in public or private financings, including: Bausch Health, Coap Tech, Innov Heart, Perimeter Medical. Read More

In the clinic for Jan. 27, 2022

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

Other news to note for Jan. 27, 2022

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Bioventix, Fluxion, FX Solutions, Materacor, Medtronic, Perceptive Solutions, Titan Medical. Read More

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