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Wiz.AI

AI-driven protocol design, data management, and document automation for clinical trials with real-time compliance tracking.

Solution by Taimei Technology
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Overview

Wiz.AI is an AI platform for clinical trials developed by Taimei Technology, designed to pioneer the future of intelligent clinical research. It unifies modular AI agents, an end-to-end platform, and a self-optimizing data framework to support seamless workflows from protocol drafting through to clinical operations — all built on real clinical expertise rather than generic AI.

The platform is purpose-built for lean clinical teams seeking enterprise-grade impact. Wiz.AI integrates Taimei Trials SaaS capabilities with autonomous decision engines, enabling organizations to deploy intelligent agents across their clinical trial workflows quickly and compliantly. It is fully compliant with global regulatory standards and offers standardized, fast-to-deploy configurations.

Core Platform Architecture

  • Modular AI Agents: Specialized modules address distinct clinical trial needs, including Wiz ProtocolCraft for protocol design and Wiz DocuSync for document management.
  • End-to-End Platform: Integrates Taimei Trials SaaS capabilities with autonomous decision engines, enabling seamless workflows from protocol drafting to clinical operations.
  • Data Language Action (DLA): A self-optimizing framework that evolves through real-time data feedback and federated learning, enabling the system to act intelligently based on incoming data.

Wiz-iDM: Intelligent Data Management

  • Transforms clinical protocols into live databases in as little as 72 hours, with a focus on quality, compliance, and control.
  • AI-Driven Protocol Parsing & CRF Automation: Automatically interprets protocols and generates Case Report Forms.
  • Data Validation Plan Automation: Streamlines the creation and management of data validation rules.
  • Intelligent Real-Time Data Review: Continuously monitors and reviews clinical data as it is collected.
  • CRF Miner & Adaptive Library Integration: Leverages an adaptive library to improve CRF design and reuse.
  • Seamless EDC Integration: Connects directly with electronic data capture systems for uninterrupted data flow.

Wiz-iCTA: Intelligent Clinical Trial Administration

  • Automates classification, metadata capture, quality control, and completeness tracking to ensure consistent document quality and keep studies inspection-ready at every stage.
  • AI Classification: Automatically categorizes clinical trial documents with precision.
  • Metadata Extraction: Captures and structures key document metadata without manual effort.
  • AI-Powered Quality Control: Applies intelligent checks to maintain document integrity and GCP compliance.
  • Completeness Tracking: Monitors document completeness across the trial lifecycle.
  • Operational Efficiency: Reduces manual administrative burden, enabling teams to achieve audit readiness in minutes.

Why Wiz.AI

  • Built on real clinical expertise, not generic AI models.
  • Standardized and fast-to-deploy configurations suitable for rapid adoption.
  • Fully compliant with global regulatory standards.
  • Designed for lean teams while delivering enterprise-scale impact.

Wiz.AI is developed by Taimei Technology, a company with an established suite of clinical data management and clinical operations solutions including EDC, RTSM, eCOA, CTMS, and eTMF. The platform is available for demonstration and is supported by dedicated sales and product hotline contacts for prospective customers globally.

Meta

Domain
Clinical Trial Management
Subdomain
Clinical Data Review & Monitoring
Software type(s)
AI Agent
Deployment type(s)
Cloud / SaaS
Industry vertical(s)
PharmaBiotechCRO
Development stage(s)
Clinical
Target user(s)
Research ScientistQA / Regulatory AffairsClinical / Diagnostic ProfessionalIT / Systems Admin / Data Engineer
Compliance standard(s)
GxPICH
Tag(s)
Uses AI