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Enterprise Layer Intelligence
Categories/Healthcare & Life Sciences/Kenosha AI
Kenosha AI

Kenosha AI

Founded 2024

Search clinical research documents, regulatory guidance, and automate routine trial study workflows

You can use Kenosha AI to query standard operating procedures, study files, and global regulatory rules for clinical trials. The system links directly to SharePoint folders to answer questions about compliance and trial protocols with page-level citations. It connects to clinical guidance from more than 135 countries and agencies like the FDA, EMA, and ICH. In addition, teams can search trial registries, generate standard responses for vendor questionnaires, and track operational logs like protocol deviations and enrollment records without relying on spreadsheets.

What Kenosha AI does

Query internal clinical trial SOP documentsCompare regulatory guidelines across different countriesSearch historical clinical trials by endpoints and biomarkersGenerate audit-ready logs for protocol deviationsDraft standard compliance answers for RFIs and RFPsRetrieve source citations for regulatory questionsDirect natural language querying across SOPs and SharePoint study foldersPage-level citations and direct links to original reference documentsRegulatory knowledge covering guidance across 135 countries and agenciesSearch index of over 500,000 clinical trial records from ClinicalTrials.govAutomated drafting of RFI and RFP questionnaire responsesAutomated tracking for protocol deviations and issue escalation logsEnterprise data isolation hosted on Microsoft Azure

Frequently asked

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Kenosha AI, ProChat, RegChat, clinical research, CRO, biopharma, regulatory guidance, SOPs, ClinicalTrials.gov, ICH, FDA, protocol deviations, clinical trials, study documents