Factify Pharma Suite
AI-Powered Pharmaceutical Research & Compliance
Comprehensive AI platform for pharmaceutical research, regulatory documentation, and clinical trial management. From preclinical studies to regulatory submissions.
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Pharmaceutical AI That Delivers
From research data management to regulatory submissions, Factify Pharma Suite automates the entire pharmaceutical documentation lifecycle while maintaining GxP compliance and full audit trails.
65% Faster CTD Processing
Automated documentation updates and regulatory monitoring.
GxP Compliant
21 CFR Part 11, full audit trails, and version control.
98% Entity Accuracy
Industry-trained NLP for active ingredients and indications.
Three Integrated Pharma Solutions
Each module addresses specific pharmaceutical research challenges, working together as a unified platform.
Pharma Research
Accelerate pharmaceutical research with intelligent data management. Automated classification, NLP-powered analysis, and seamless integration with laboratory systems.
- Research data aggregation from clinical studies
- Automated data classification and OCR extraction
- NLP-powered analysis with 65% time reduction
- Intelligent document retrieval system
- Advanced entity recognition for pharma terminology
Regulatory AI (CTD-AI Suite)
Automated regulatory documentation maintenance. Monitor ICH, EMA, and FDA guidelines with proactive compliance management and specialized AI agents.
- Automated monitoring of regulatory guideline changes
- AI-driven documentation update identification
- Proactive risk detection and compliance management
- Specialized agents: Safety, Regulatory, Research, Compliance
- GxP-compliant audit trails and version control
Study Management
End-to-end preclinical trial management. From study planning through protocol definition to final data analysis with AI-powered quality assurance.
- Structured study planning and resource management
- Automated protocol definition and validation
- Intelligent workflow management system
- Real-time data quality monitoring
- 21 CFR Part 11 compliance
AI Research Platform
An integrated AI platform revolutionizing pharmaceutical R&D. From literature discovery to regulatory submission preparation - eight powerful modules working in harmony.
Systematically generate and prioritize research hypotheses, accelerate evidence synthesis, and seamlessly bridge research findings to regulatory submissions.
Integrated Research Workflow
Eight modules connected through a unified knowledge layer
Dashboard
Central Command Center
Discovery Hub
Intelligent Literature Exploration
Evidence Synthesis
PRISMA-Compliant Systematic Reviews
Hypotheses
AI-Powered Hypothesis Generation
Prioritization
Multi-Criteria Decision Analysis
Study Proposals
Protocol Generation
Research Notes
Collaborative Knowledge Management
CTD Bridge
Regulatory Submission Preparation
Eight Integrated Modules
Dashboard
Central Command Center
Real-time overview of all research activities, KPIs, and project status. Your single source of truth for pharmaceutical R&D.
- Real-time KPIs and metrics
- Project status overview
- Team activity feed
- Alert and notification center
Discovery Hub
Intelligent Literature Exploration
AI-powered literature search across PubMed, clinical trials, and proprietary databases with semantic understanding.
- Semantic search across multiple databases
- Automatic relevance scoring
- Citation network analysis
- Saved searches with alerts
Evidence Synthesis
PRISMA-Compliant Systematic Reviews
Automated systematic review workflows following PRISMA guidelines with AI-assisted screening and data extraction.
- PRISMA-compliant workflow
- AI-assisted abstract screening
- Automated data extraction
- Risk of bias assessment
Hypotheses
AI-Powered Hypothesis Generation
Generate and evaluate research hypotheses based on evidence synthesis and knowledge graph connections.
- AI-generated hypothesis suggestions
- Evidence strength scoring
- Knowledge graph visualization
- Hypothesis versioning and tracking
Prioritization
Multi-Criteria Decision Analysis
Systematic prioritization of research directions using configurable criteria and stakeholder input.
- Weighted scoring models
- Stakeholder voting system
- Scenario analysis
- Decision audit trails
Study Proposals
Protocol Generation
AI-assisted study protocol generation with templates, regulatory alignment, and feasibility assessment.
- Protocol template library
- Regulatory requirement checker
- Feasibility assessment tools
- Budget estimation
Research Notes
Collaborative Knowledge Management
Structured note-taking with AI tagging, cross-referencing, and knowledge base integration.
- AI-powered tagging
- Cross-reference suggestions
- Team collaboration features
- Version history and comments
CTD Bridge
Regulatory Submission Preparation
Seamless connection to CTD-AI Suite for preparing regulatory submissions from research findings.
- Evidence package export
- CTD module mapping
- Gap analysis for submissions
- Audit-ready documentation
Transform pharmaceutical research from reactive literature reviews to proactive, AI-driven hypothesis generation. Connect the dots across millions of publications, clinical trials, and internal data to uncover novel therapeutic opportunities faster.
Specialized AI Agents
Purpose-built AI agents work together to automate complex pharmaceutical workflows.
Safety Agent
Monitors safety signals and adverse event patterns across studies
Regulatory Agent
Tracks guideline changes from ICH, EMA, FDA, and other authorities
Research Agent
Analyzes research data and identifies patterns in clinical outcomes
Compliance Agent
Ensures documentation meets GxP and regulatory requirements
Platform Capabilities
Enterprise-grade infrastructure designed for pharmaceutical research requirements.
NLP & Entity Recognition
98% accuracy in active ingredient recognition, 95% in indication identification.
GxP Compliance
Full audit trails, version control, and regulatory documentation support.
Process Automation
65% reduction in CTD processing time through intelligent automation.
System Integration
RESTful APIs connect to LIMS, CTMS, and existing pharma infrastructure.
Predictive Analytics
AI-driven insights for research planning and risk assessment.
Collaboration Tools
Interdisciplinary team coordination with real-time updates.
Accelerate Your Pharmaceutical Research
See how Factify Pharma Suite can reduce documentation time by 65% while improving compliance.
See Factify Pharma in Action
From research to regulatory compliance
For Pharma Companies
Schedule a personalized demo and see how we can accelerate your research and compliance workflows.
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