Valiqa
AI generator for audit-ready validation protocols
Details
- Target Audience
- QA EngineersEnterprisesManufacturers
- Pricing
- Subscription from $149
- Platforms
- Web
- Featured in
- Best Tools for Manufacturers
About Valiqa
Valiqa generates audit-ready IQ, OQ, PQ, DQ, PPQ, CSV, PV, and TQ validation protocols for regulated manufacturing. Not templates. Actual protocols with real test steps, acceptance criteria, and regulatory references specific to your equipment. Who it's for: quality engineers, validation engineers, and QA managers at medical device, pharmaceutical, biotech, and food manufacturing companies. What you get: - 10 protocol types: IQ, OQ, PQ, DQ, PPQ, CSV, PV, TQ, VMP, PFMEA - Full test steps with acceptance criteria and pass/fail fields - Regulatory references mapped to your standards (FDA 21 CFR 820, ISO 13485, EU MDR, MDSAP, ICH Q7, and 15 more across 4 industries) - PFMEA following AIAG-VDA with Action Priority (H/M/L) - Part 11 audit trail - Traceability matrix linking requirements to test steps - DOCX export in your company format - Validation Master Plan generator What makes it different: most tools are document management systems. Valiqa generates the content. Describe your equipment, get a full protocol. Real test steps, real acceptance criteria. Not a blank form with headers. A protocol that used to take 2-3 days now takes under 30 minutes. 14-day free trial. No credit card required.
Product Insights
Valiqa is a web-based AI automation platform that generates equipment-specific validation protocols for regulated manufacturing sectors. It provides comprehensive documentation including IQ, OQ, and PQ protocols with automated regulatory mapping for legal and compliance standards.
- Generates 10 distinct protocol types including VMP, PFMEA, and Traceability Matrices.
- Integrated regulatory mapping for FDA 21 CFR 820, ISO 13485, and EU MDR standards.
- Automated content generation featuring specific test steps and acceptance criteria.
- DOCX export capabilities compatible with existing company formatting and Part 11 audit trails.
Ideal for: QA Engineers and Manufacturers at medical device and pharmaceutical companies requiring audit-ready validation documentation for regulated equipment.
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Built this after spending years watching validation engineers write IQ/OQ/PQ protocols in Word. Describe your equipment, get a full protocol in minutes. Happy to answer questions here.