Release Faster. Stay Compliant. One Platform.
The only LIMS + Lab Execution System with compliance built in, AI-ready workflows, and no-code integrations—so you release lots faster without the integration headaches.
Trusted by pharma QC labs, CDMOs, and global lab networks
Why Regulated Labs Choose NexaQore
Built for labs where every deviation costs time and money. Here’s how we help you reduce risk and speed up release.
Execute Every Lab Workflow, End-to-End
From sample receipt to final release, manage complete laboratory workflows with precision and traceability.
- End-to-end lab workflow execution
- Procedure templates and standardization
- Result entry with real-time validation
- Exception management and resolution
- Review by Exception workflows
Compliance Built Into Every Action
21 CFR Part 11 compliant by design. Every action is audited, verified, and traceable with ALCOA+ principles.
- Centralized audit trails with checksums
- 21 CFR Part 11 compliance
- ALCOA+ verification and validation
- AQL standards enforcement
- 7-stage Laboratory Investigation Reports
Release Faster with Review by Exception
Accelerate product release cycles by focusing reviewer attention only where it matters most.
- Automated review workflows
- Exception-based routing
- Lot release by exception
- Sample review by exception
- Configurable approval routes
Agent-Ready, No-Code Integration
Connect instruments, systems, and data sources without code. Future-ready for AI agents and real-time data capture.
- Direct TCP/IP instrument integration
- File-based and hybrid integration
- No-code parsing and transformation
- Agent-ready APIs and event streams
- Integration marketplace and extensible connectors
Smart Assignment & Master Data Libraries
Advanced algorithms balance workload and resources automatically. Master data libraries let you reuse and scale configurations & build complex structures in minutes, not days.
- Automatic assignment based on user load and available resources
- Master data libraries for Analysis (methods, compendial analyses, specifications)
- Master data libraries for Reports (templates, COA, LIR, custom report definitions)
- Master data libraries for Integrations (connectors, mappings, transformation rules)
- Algorithm-driven generation and validation for specs, methods, and templates
Future-Ready Automation & Control
Orchestrate complex workflows with event-driven architecture. Built for automation today and AI augmentation tomorrow.
- FUSE Autoflows and event-driven architecture
- Workflow builder and scheduling
- Inbound/Outbound messaging (SQS/RabbitMQ)
- REST APIs, Webhooks, and notifications
- Veeva Vault and ecosystem integrations
Built for Your Role
Whether you’re in the lab, QA, or IT—see the part of the platform that matters most to you.
FUSE Integration Platform
Future-ready, agent-friendly integrations. Connect LIMS to instruments and systems with no code—and prepare for AI-driven workflows.
- Integration Marketplace
- No-Code Instrument Integration
- Agent-Ready APIs & Events
- Real-time Data Capture
Quality & Compliance
21 CFR Part 11 compliant by design with ALCOA+ principles, comprehensive audit trails, and complete investigation workflows.
- Centralized Audit Trails
- 21 CFR Part 11 Compliance
- Exception Management
- Laboratory Investigations
Lab Execution System (LES)
Execute every lab workflow from procedure template to final release with built-in validation, approvals, and exception handling.
- Procedure Templates
- Workflow Execution
- Approvals & Exceptions
- Resource Management
Material & Instrument Management
Complete material lifecycle management with GMP compliance, inventory tracking, and threshold alerts. Instrument Management built in: calibration, preventive maintenance, and performance checks, ready to use with end-to-end tracking of instrument usage across the system.
- Material Lifecycle & Inventory Management
- GMP Compliance & Threshold Alerts
- Instrument Management: Calibration, Preventive Maintenance, Performance Checks (built-in, ready to use)
- End-to-end tracking of Materials & Instruments usage across the system
LIMS + LES Capabilities for Regulated Labs
From sample to release—compliance, automation, and future-ready integration in one platform.
- Sample Management with Review by Exception
- Lot Management with Release by Exception
- Stability Management
- Environmental Monitoring
- End-to-end lab workflow execution
- Procedure Templates
- Result Entry with validation
- Exception Management
- Review by Exception
- Release by Exception
- Centralized Audit Trails
- End-to-End Audit Trails with checksums
- 21 CFR Part 11 Compliance
- ALCOA+ Verification
- AQL Standards
- Laboratory Investigation Reports (7-stage LIR workflow)
- Material & Reagent Management
- Inventory Lifecycle
- Consumption, Returns, Destruction
- Specifications Management
- Inventory Threshold Alerts
- Instrument Lifecycle
- Calibration & PM
- Performance Checks
- Direct TCP/IP Integration
- File-Based Integration
- No-Code Parsing
- Hybrid Integration
- Real-time data capture
- COA Generation
- LIR Reports
- Out of the box Report Templates
- Query Manager for custom queries
- PDF Generation
- Role-Based Dashboards
- Visual Query Builder for custom queries
- FUSE Autoflows
- Event-Driven Architecture
- Workflow Builder
- Scheduling
- Inbound/Outbound Messaging (SQS/RabbitMQ)
- Integration Marketplace
- REST APIs, Webhooks, Slack, Email
- Veeva Vault Integration
- Visual Label Designer
- Barcode & QR Code Support
- Label Templates
- User Lifecycle Management
- RBAC+
- Functional Privileges
- Menu Control
- API Permissions
- Session & License Management
- Account Lockout
- Rate Limiting
- XSS / CSRF Protection
- Security Audit Logs
- Configurable Approval Routes
- Electronic Signatures
- Multi-Step Approvals
- Approval History
- Per-Object Configuration
- Compendial Analyses
- Analysis Templates
- Label Templates
- Report Templates
- Material Specifications
- Visual Query Builder
- Notification System (Email + In-App)
- System Administration
- Data Import / Export
See How QC Labs Like Yours Release Faster
Get a 15-minute walkthrough built around your lab’s biggest pain—compliance, release cycles, or integrations. No pitch, just value.
Trusted by pharma QC labs, CDMOs, and global lab networks