{"id":2195,"date":"2025-12-09T12:40:54","date_gmt":"2025-12-09T12:40:54","guid":{"rendered":"https:\/\/wptest.raylytic.com\/?page_id=2195"},"modified":"2026-03-18T11:03:47","modified_gmt":"2026-03-18T11:03:47","slug":"imaging-core-lab-services","status":"publish","type":"page","link":"https:\/\/www.raylytic.com\/en\/imaging-core-lab-services\/","title":{"rendered":"Imaging Core Lab Services"},"content":{"rendered":"\t\t
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Imaging Core Lab Services for Medical Device Trials<\/b><\/h1>\t\t\t\t<\/div>\n\t\t\t\t
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RAYLYTIC delivers advanced radiographic analysis and fit-for-purpose imaging core lab services to aid medical device manufacturers and CROs in generating high-quality, regulatory-grade evidence.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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Discover Our Imaging Core Lab Services<\/h2>\t\t\t\t<\/div>\n\t\t\t\t
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Designed to work seamlessly alongside the RAYLYTIC Platform, our core lab services deliver the scientific, clinical, and operational expertise your study needs for success. Trusted by over 30 medical device manufacturers across diverse regulatory pathways, we bring proven experience to every trial we support.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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What We Offer<\/h3>\r\n <\/div>\r\n\r\n \r\n
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Imaging Endpoint Definition & Standardization<\/p>\r\n <\/i>\r\n <\/div>\r\n <\/div>\r\n

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We support you in defining the measurement methods that lead to your imaging endpoints, and advise you on the selection of relevant parameters. In doing so, we ensure that the endpoints are clinically meaningful, measurable, and justifiable for your specific study \u2014 grounded in current literature and established standards. Please note: We do not develop study protocols or regulatory documentation, and we are not involved in direct communication with regulatory authorities.<\/p>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n\r\n \r\n

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AI-Based Quantitative Radiographic Analysis<\/p>\r\n <\/i>\r\n <\/div>\r\n <\/div>\r\n

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Extract quantitative imaging endpoints, device performance metrics (fusion, subsidence, alignment), and morphoanatomical measurements with precision. Our AI-assisted tools accelerate analysis by 50% compared to traditional manual workflows while maintaining accuracy and reproducibility.<\/p>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n\r\n \r\n

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Radiologist Network for Qualitative Image Analysis<\/p>\r\n <\/i>\r\n <\/div>\r\n <\/div>\r\n

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Independent blind central image review conducted by experienced, board-certified radiologists. Direct access to senior experts\u2014not ticket queues or account managers. Our network ensures unbiased evaluation with standardized protocols and responsive, personalized support.<\/p>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n\r\n \r\n

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Image Quality & Site Compliance Monitoring<\/p>\r\n <\/i>\r\n <\/div>\r\n <\/div>\r\n

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Every image is reviewed to ensure consistency in quality and protocol compliance. Real-time, proactive feedback to sites prevents costly downstream issues\u2014unlike traditional reactive approaches that discover problems only after expensive rework is required.<\/p>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n\r\n \r\n

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Clinical Trial Imaging Infrastructure<\/p>\r\n <\/i>\r\n <\/div>\r\n <\/div>\r\n

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Proprietary image management system with native EDC integration\u2014imaging data lives within your study database, not in separate silos, including imaging eCRFs. No time-consuming reconciliation or manual data transfers. Full audit trail and regulatory compliance built in.<\/p>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n\r\n \r\n

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Imaging Review Charter Development<\/p>\r\n <\/i>\r\n <\/div>\r\n <\/div>\r\n

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Agile charter development tailored to your trial's unique needs\u2014imaging modalities, assessment methods, and protocols for ethics\/regulatory submission. Based on literature review and regulatory guidance, with flexibility to adapt mid-study without enterprise bureaucracy.<\/p>\r\n <\/div>\r\n <\/div>\r\n <\/div>\r\n\r\n <\/div>\r\n<\/section>\r\n\r\n