Intellect QMS
AI-powered no-code quality management for manufacturing and life sciences
Founded
2000
Starting Price
$19,000
Category
Manufacturing & ERP
Last updated April 27, 2026
About Intellect QMS
Intellect QMS is an AI-powered quality management system designed for manufacturing, life sciences, and regulated industries. The no-code platform enables teams to build custom quality workflows, automate compliance processes, and manage documents, audits, CAPA, and supplier quality without any coding. It supports over 30 applications across 9+ ISO standards.
Pros & Cons
Pros
- Highly flexible no-code platform lets non-technical users build custom quality apps
- AI Smart Analysis provides data-driven insights and root cause recommendations
- Supports 30+ pre-built applications across 9+ ISO standards
- Strong customer support with hands-on implementation assistance
- Good value compared to larger QMS platforms like MasterControl or ETQ
Key Features
No-Code App Builder
Drag-and-drop interface to create custom quality applications without programming skills
AI Smart Analysis
Built-in AI for plain-language conversations to extract data trends, root causes, and recommended solutions
Document Control
Centralized document management with version control, approval workflows, and audit trails
CAPA Management
Corrective and preventive action tracking from identification through resolution and effectiveness verification
Audit Management
Plan, schedule, and execute internal and external audits with automated finding tracking
Change Management
Structured change control processes with impact analysis and stakeholder notifications
Supplier Quality Management
Monitor and evaluate supplier performance with scorecards and qualification workflows
Pricing
Pro
$19,000/year
- Core QMS applications
- No-code app builder
- Standard support
- Cloud deployment
Premier
$29,000
Best For
Manufacturing Quality Control
Manage quality processes across production lines with automated CAPA, audit management, and nonconformance tracking
Life Sciences Compliance
Maintain FDA, ISO 13485, and GxP compliance with validated document control and training management
Supplier Quality Programs
Evaluate and monitor supplier performance with scorecards, qualification workflows, and corrective action tracking
ISO Certification Management
Prepare for and maintain ISO 9001, ISO 14001, and other certifications with integrated audit and document control
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