Cloudtheapp eQMS

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Cloudtheapp is an AI-powered, cloud-native Quality Management System (QMS) built for regulated industries including pharmaceutical, medical device, biotech, food and beverage, and manufacturing. FDA-validated under 21 CFR Part 820 (QMSR) and compliant with ISO 13485, ISO 9001, and ISO 22001, the platform gives quality teams a fully validated system without the implementation burden of legacy QMS software. The platform includes 45+ applications — CAPA, Audit Management, Document Control, Deviations, Training, Supplier Qualification, Complaints, Risk Management, and more — all configurable without code using AI-driven drag-and-drop designers. Quality teams can build, configure, and deploy new applications in minutes by describing requirements in plain language. Key capabilities include: built-in 21 CFR Part 11 audit trail across all modules, separate corrective action and preventive action workflows, AI-powered root cause analysis, electronic signatures, and a complete validation package delivered with every platform update. Unlike traditional QMS vendors, Cloudtheapp does not require expensive implementation consultants or lengthy validation projects. Organizations go live faster, configure more deeply, and scale without additional per-seat or per-module costs. Features Checklist: G2 shows a features checklist on every profile. Check every feature Cloudtheapp supports. The key ones buyers filter by in the QMS category: • Document Control • CAPA Management • Audit Management • Corrective Actions • Preventive Actions • Risk Management • Electronic Signatures • Audit Trail / Version Control • Supplier Management • Training Management • Nonconformance Management • Change Management • Reporting and Dashboards • Mobile Access • API / Integrations • Role-Based Access Control • Cloud Deployment • Validation Package / IQ OQ PQ