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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

May 24, 2022

View Archived Issues
Rapid PE Triage & Notification product

FDA gives nod to two AI solutions to speed CVD diagnoses

The transformation of cardiology continues with two U.S. FDA actions to promote the use of artificial intelligence (AI): a 510(k) clearance for Rapidai Inc.’s pulmonary embolism (PE) triage and notification product and breakthrough device designation for Anumana Inc.’s pulmonary hypertension (PH) early detection algorithm. Read More
Patient holding Cordella reader over heart

Endotronix reports early data for heart failure sensor

Endotronix Inc. reported positive data from the SIRONA 2 clinical trial evaluating safety and efficacy of its Cordella pulmonary artery pressure sensor system in New York Heart Association (NYHA) class III heart failure (HF) patients.  Read More
Regulatory-US-FDA-HQ.png

Implementation timelines a key concern regarding FDA proposal to align with ISO 13485

The U.S. FDA’s proposal to restructure the Quality System Regulation (QSR) with ISO 13485, the international quality system standard, is a major shift for affected industry, but there are strictly administrative issues associated with this proposal. Several of those who have commented to the docket have expressed misgivings as to the proposed 12-month compliance deadline upon issuance of a final rule. Read More
How it works diagram: Step 1 task image displayed, Step 2 eye tracking, Step 3 cognitive scoring

Otsuka to market Ai-Brainscience’s eye-tracking cognitive test app in Japan

Otsuka Pharmaceutical Co. Ltd. and Ai-Brainscience Inc. signed an exclusive sales agreement for Japan that will see Otsuka market Ai-Brainscience’s eye-tracking application to test for cognitive function. The eye-tracking app, AiBS-01, could become the first dementia diagnosis application to receive regulatory approval in Japan. Ibaraki, Japan-based Ai-Brainscience (AiBS) is developing devices that use the eye-tracking based cognitive assessment test to detect early dementia beyond the conventional assessment methods performed by specialists. Read More
U.K. flag on stethoscope

NICE inks guarded recommendation for aortic root support for Marfan syndrome patients

Those who are burdened with Marfan syndrome face a lifetime of multi-organ system issues including potential aortic aneurysm, but help may be on the way in the U.K. The National Institute of Health and Care Excellence (NICE) has issued a recommendation that these patients be treated with personalized external aortic root support (PEARS) to treat both aortic root expansion and aortic dissection, although the agency indicated that this procedure is not quite ready for routine use in the National Health Service. Read More

Appointments and advancements for May 24, 2022

New hires and promotions in the med-tech industry, including: CN Bio, Coopervision, Know Labs, Komodo Health. Read More

Financings for May 24, 2022

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

In the clinic for May 24, 2022

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

Other news to note for May 24, 2022

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aidoc, Central Medical Supply, Gleamer, Helping Hands, Pancryos, PPD Homecare, Zymo. Read More

Regulatory actions for May 24, 2022

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Anumana, Caredx, Cytek Biosciences, Inheart, Invenio Imaging, Rapidai. Read More

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