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Start delivering personalised medicine insights at scale with Vitae Evidence.
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Getting Started, Release notes and Product Guides
We co-design with innovative clinics and Digital Health teams to create quality solutions embedded into Healthcare Providers' workflow.
MDT unites care professionals from different disciplines and institutions to jointly decide upon the best possible treatment.
In this way decisions taken for the patients are based on all available information and scientific evidence where each member can provide their specific expertise.
"Due to a dramatic increase in demand, with only minor increases in capacity, there is not enough time to discuss the more complex patients"
Vitae Evidence leverages AI and digital health to help MDTs deliver more efficient integrated care.
By integrating with your electronic medical records and your standard of care guidelines, we'll compute a list of biomarker tests and treatment top recommendations matching each individual patient profile. Patients that have a standard of care treatment pathway will be effectively triaged from patients without standard options.
Our AI-assisted Patient Pathway standalone or SMART-on-FHIR module will help you build an interactive 1-page personalised, evidence-based healthcare journey in the context of clinical guidelines and experimental, actionable evidence. All participants quickly grasp important past events and future options, removing silos between care organizations, and engaging the patient.
Vitae Evidence's algorithms perform a comprehensive bibliographic, bioinformatics and real-world outcomes search. This enables you to provide the evidence basis and a patient relevance argumentation for your care decision, according to Evidence-Based Medicine best practices and Real-World Research principles.
Improve patient participation and molecular biology expertise with Coremine Vitae's Case Teams.
From onboarding to reporting, Coremine Vitae simplifies the process for you, and provides an easy roll out to all your workforce and your populations.
Our regulatory processes for Software as Medical Devices
GDPR Compliant
Registered CE-Mark at NoMA (MDD Class I)
Exempted from UK MHRA registration until June 2023
We apply ISO 13485 Quality Management System
We leverage ISO/IEC 27001 certified hosted solutions
Start delivering personalised medicine insights at scale. Collaborative learning powered by AI.
