Physician's Weekly
JUNE 19, 2025
Researchers have engineered a portable “lab‑in‑tube” (LIT) assay that detects Mycobacterium tuberculosis (Mtb) DNA directly from blood, saliva, or sputum in less than 60 minutes at a relatively low cost, according to a study published in Science Translational Medicine.
Annals of Family Medicine
NOVEMBER 20, 2024
Objective The aim is to evaluate the feasibility of an instructed large language model (LLM) to assist with human synthesis such as temporal topic search and screening by citation in systematic reviews for Brain-Heart-Interconnectome (BHI) to support reporting guidelines, such as CONSORT and SPIRIT.
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The Medical Futurist
JUNE 21, 2025
The 80-year-old Ray Flynn lost his central vision entirely, but with the help of the retinal implant, he could make out shapes on the computer screen. Running trials in animals will take additional engineering and safety tests. Experts even say the eye is an ideal place to start for the first clinical use of CRISPR.
Imperial Center Family Medicine
MAY 5, 2025
It’s similar to revving a car engine for too long while staying still. People with clinical depression often have elevated cortisol levels, potentially leading to high blood pressure over time. However, chronic stress keeps your body in a continuous state of high alert.
GeriPal
MAY 5, 2022
Was there any mention about the impact that hearing loss has in communication or what we should do about it in clinical practice? Screening for addressing hearing loss should be an integral part of what we do in geriatrics and palliative care, but it often is either a passing thought or completely ignored. I’m guessing not.
FDA Law Blog
OCTOBER 10, 2023
airport security screening), or surgical procedures, as well as the potential for reoperation or revision of the implant. Non-Clinical Recommendations The draft guidance highlights non-clinical review areas that are generally relevant across 510(k) Implants and offers recommendations for performance data to include in a 510(k) submission.
FDA Law Blog
JULY 10, 2023
When a firm submits a Traditional 510(k), FDA first performs the acceptance review to determine whether a submission is administratively complete, or passes the technical screening for an electronic submission submitted using the eSTAR. An AI letter typically begins with the most significant deficiencies.
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