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Frequently Asked Questions

NOESIS prioritizes data security with role-based access management, comprehensive audit trails, high-strength encryption protocols, and compliance with industry standards, providing peace of mind for organizations handling sensitive information.
NOESIS is a multi-tenant SaaS platform. Which means it can be utilized by pharmaceutical organizations as well as contract research organizations (CROs). CROs use different NOESIS tenants for each of their customers with each tenant having its own configurations and integrations. NOESIS architecture ensures the data remains physically and logically separated at all times.
NOESIS can automate case intake from a wide range of sources including structured forms, scanned documents, handwritten documents, spreadsheets, emails, attachments, literature abstracts, and literature full-text articles.
NOESIS boasts over 98% accuracy in structured document data extraction and a BLEU score of over 0.6 for auto-translation, ensuring highly accurate and standardized data for downstream processing. NOESIS achieved an F1 score of more than .76 in a recent customer pilot for processing and extracting relevant safety information from Literature full-text articles.
Yes, NOESIS is designed for seamless integration with various safety systems and databases, offering flexibility and adaptability to meet the needs of different organizations and workflows. NOESIS uses different integration methods such as APIs, sFTP for integrating with upstream or downstream systems. NOESIS provides out-of-the-box integration with active directories such as okta and Azure AD for single sign-on.
NOESIS is equipped with proprietary techniques for language-agnostic data extraction, as well as accurate language translations at lower costs, ensuring language barriers are not a hindrance in case management processes.