
Cloudtheapp Pricing
Tailored Plans - Built-in Value - Endless Possibilities
Standard
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Deploy 50+ Applications from Cloudtheapp Store
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Configure Deployed Applications with Best in Class Designer Tools
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Create New Applications with Cloudtheapp Thunder – Your AI Assistant for Process Digitalization
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Cloudtheapp Analytics – Build Unlimited Graphs and Dashboards and Get Better Insights on Your Data
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Deploy Unlimited Environments (Dev, Sandbox, Val, Live)
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Best in Class Configuration Management – Copy Configured Applications from One Environment to the Other with a Click of a Button
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Seamless Collaboration with Suppliers and External Parties
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QR Code Record Submissions by External Users
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Get Unmatched Support with Cloudtheapp: Always Here, Always Reliable!
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Access to Online Training Video Library
Advanced
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All Standard Features
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Validated Platform – Validation Package for Every Platform Update
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Electronic Signature
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Audit Trail
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Transaction History Tracking
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Forced Authentication (on Save and Route)
Enterprise
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All Advanced Features
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Single Sign On (SSO)
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Integrations API
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The Sky is the limit!
Connected Team
(for your Suppliers)
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Number of Active Users [3 Users max]
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Centralized Assignments Portal and Seamless Collaboration
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Access to Online Training Video Library
Deploy The Applications You Need - All In One Place
Application | EQMS | FSMS | SQM | EHS | RIM | ERM | LMS | MES | SV | LCS |
---|---|---|---|---|---|---|---|---|---|---|
Advanced Inspections | ✓ | ✓ | ✓ | ✓ | ||||||
Adverse Events | ✓ | |||||||||
Aspects and Impacts | ✓ | |||||||||
Audits | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ||||
Batch Records | ✓ | ✓ | ✓ | ✓ | ||||||
Bill of Materials | ✓ | ✓ | ✓ | |||||||
Calibration and Maintenance | ✓ | ✓ | ✓ | ✓ | ||||||
Change Management | ✓ | ✓ | ✓ | ✓ | ✓ | |||||
Chemical Management | ✓ | ✓ | ✓ | |||||||
Complaints | ✓ | ✓ | ✓ | |||||||
Compliance Requirements | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ||||
Corrective and Preventive Actions | ✓ | ✓ | ✓ | ✓ | ||||||
Customer Returns | ✓ | |||||||||
Customers and Products | ✓ | ✓ | ✓ | ✓ | ||||||
Defects | ✓ | ✓ | ||||||||
Design Controls | ✓ | ✓ | ||||||||
Deviations | ✓ | ✓ | ||||||||
Device Master Records | ✓ | |||||||||
Documents | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | |
Engineering Change | ✓ | |||||||||
Enterprise Risk Management | ✓ | ✓ | ||||||||
Equipment | ✓ | ✓ | ✓ | ✓ | ||||||
FMEA | ✓ | ✓ | ✓ | |||||||
General Records | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ||
HACCP | ✓ | |||||||||
Hazard Analysis | ✓ | |||||||||
Incidents | ✓ | |||||||||
Inspections | ✓ | ✓ | ✓ | ✓ | ||||||
Inventory Management | ✓ | ✓ | ||||||||
Issue Tracking | ||||||||||
Lab Testing | ✓ | ✓ | ✓ | |||||||
Learning | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | |
Management Review | ✓ | ✓ | ||||||||
Material Lot Records | ✓ | ✓ | ||||||||
Nonconforming Material | ✓ | ✓ | ✓ | |||||||
Objectives and Targets | ✓ | |||||||||
Out of Specification | ✓ | ✓ | ✓ | |||||||
Permit to Work | ✓ | |||||||||
Post Market Surveys | ✓ | |||||||||
Processes | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ||
Quality Issues | ✓ | ✓ | ✓ | |||||||
Receiving | ✓ | ✓ | ||||||||
Regulatory Dossiers and Submissions | ✓ | |||||||||
Risk Assessments | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ |
Shipping | ✓ | |||||||||
Supplier Qualification Management | ✓ | ✓ | ||||||||
Suppliers and Materials | ✓ | ✓ | ✓ | ✓ | ✓ | |||||
Tasks | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ✓ | ||
Validation | ✓ |