Cloudtheapp Information

Cloudtheapp is a validated, cloud-native quality and compliance platform for life sciences and regulated manufacturing. Intelligent assistance helps teams configure processes and reduce manual work, with quality professionals still in control of every GxP decision. Quality that adapts to you. Not the other way around. We help Quality, RA, Operations, and CSV teams run document control, CAPA, deviations, change control, training, supplier quality, audits, complaints, risk, design controls, and 60+ applications on one pre-validated AWS platform. Every platform update ships with a validation package. Move configurations from Dev to QA to Production in seconds. Collaborate with suppliers and external parties inside the system at no extra cost. Built for industries where quality is non-negotiable: pharmaceutical, medical device, biotechnology, food manufacturing, chemical, and broader manufacturing. What buyers use us for • Pre-validated eQMS with 21 CFR Part 11 controls, audit trails, and e-signatures • Medical Device Pre-Market Kit (design controls, DHF, ISO 14971, 510(k)-oriented workflows) • Medical Device Post-Market Kit (complaints, MDR/vigilance clocks, CAPA, PMS/PMCF evidence) • Fast-Track implementation: focused first release configured and live in as little as 30 days • Partner Program for independent consultants and consulting firms • No-code designers plus intelligent assistance to stand up and adjust processes without multi-year custom projects. • How control works Assistance can draft, suggest, and accelerate configuration. Nothing becomes a controlled GxP record until your trained users review and approve under your procedures. Part 11 audit trail and e-signature rules still apply. Request a demo: https://www.cloudtheapp.com/demo/ Pre-Market Kit: https://www.cloudtheapp.com/industries/medical-device-pre-market Post-Market Kit: https://www.cloudtheapp.com/industries/medical-device-post-market Partners: https://www.cloudtheapp.com/partners