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Image: Alzheimer’s pathology can start 15 to 20 years before symptoms, and validated tools that reach patients earlier help pave the way for earlier detection. (Image Credit: Adobe Stock)

Alzheimer’s Blood Test Becomes First FDA-Cleared Option for Adults as Young as 40

An Alzheimer’s blood test becomes the first cleared by FDA for symptomatic adults as young as 40. More...
21 Aug 2026
Image: The collaboration will give pharma companies, diagnostic providers, and CROs a streamlined way to develop and operationalize IHC-based companion diagnostics programs.

AI-Powered Pathology Collaboration Supports Companion Diagnostic Development

Imagene AI joined the Proscia Ready alliance to integrate its H&E screening and IHC image-analysis tools with Proscia’s Concentriq platform. More...
21 Aug 2026
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Simple Whole-Blood Screen Identifies Elevated Bile Acids Linked to Liver Disease

A whole-blood test rapidly flags elevated bile acids before routine liver markers rise. More...
20 Aug 2026
Image: Aletta is designed to autonomously perform diagnostic blood collection using multimodal imaging and advanced control. (Photo courtesy of Vitestro)

Autonomous Robotic System Receives FDA Authorization for Blood Collection

Vitestro’s Aletta, an Autonomous Robotic Phlebotomy Device (ARPD), received De Novo authorization from the U.S. FDA. More...
20 Aug 2026
Image:  Estimates suggest that 30–50% of CKD cases go undiagnosed in high‑income countries, with even higher proportions likely in middle‑ and lower‑income countries (Image Credit: Shutterstock)

Routine Urine Protein Testing Identifies Undiagnosed Chronic Kidney Disease

New findings reveal up to half of CKD cases go undetected, urging routine urine protein testing to improve early detection. More...
20 Aug 2026
Image: Aletta is designed to autonomously perform diagnostic blood collection using multimodal imaging and advanced control. (Photo courtesy of Vitestro)

Autonomous Robotic System Receives FDA Authorization for Blood Collection

Vitestro’s Aletta, an Autonomous Robotic Phlebotomy Device (ARPD), received De Novo authorization from the U.S. FDA. More...
20 Aug 2026
Image: Incorporating the score into routine testing could help genetic laboratories diagnose type 1 diabetes in patients with unexplained negative MODY results (Image Credit: Adobe Stock)

Genetic Risk Score Identifies Type 1 Diabetes in MODY Testing

New data show a type 1 diabetes genetic risk score in MODY workflows helps uncover hidden type 1 cases and cuts extra tests. More...
20 Aug 2026
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