Valiqa

What Valiqa does? Valiqa is an AI-powered validation protocol generator for regulated manufacturing. It produces audit-ready IQ, OQ, PQ, DQ, and PPQ protocols, plus Validation Master Plans, in minutes instead of weeks. Who it is for? Quality, validation, and regulatory teams at medical device, pharmaceutical, biotech, and food manufacturers. Built for the small and mid-sized companies that need FDA and ISO-grade documentation without an enterprise validation-suite budget. What you get? - IQ, OQ, PQ, DQ, and PPQ protocols generated from your equipment and process details - Validation Master Plans (VMP) and requirement-traceable documentation - Output aligned to FDA 21 CFR Part 11, FDA 21 CFR Part 820, ISO 13485, GMP, and MDSAP expectations - International coverage: UK, EU, India, Korea, Mexico, Brazil, and ISO 9001 - Execution support: electronic signatures, tamper-evident audit trail, and deviation tracking on every protocol - Documents grounded in your uploaded equipment specifications, not generic boilerplate Why teams choose Valiqa? Traditional validation lifecycle platforms are expensive, slow to deploy, and built for large enterprises. Valiqa delivers the same audit-ready output in minutes, self-serve, with transparent pricing from $199/month and an instant free trial - no demo call, no sales cycle. Know your process. Prove your compliance. Ship faster.