Quality Manager
Compliance Lead- Oversees document control and regulatory compliance
- Manages CAPA processes end-to-end
- Monitors quality metrics across all sites
moon-eqms
byTemp
can you create a eQMS platform for Pharmacuetical company who has registred with US FDA. include every possible feature in the market to make it
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Quality Connected
Every document, CAPA, workflow, and approval is linked in one compliant eQMS. Sign in to manage your quality processes.
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moon-eqms · FDA-Compliant eQMS
PharmaceuticalQualityManagementReimagined
Unify document control, CAPA, approvals, and workflows in one validated platform. moon-eqms keeps your pharmaceutical operations audit-ready for US FDA 21 CFR Part 11 — while cutting quality cycle times and manual effort.
21 CFRPart 11 Ready
60%Faster Audits
5Core eQMS Modules
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Interconnected Quality
One molecule, five quality modules in motion
Hover any node to expand its cluster and dim the rest. Click to zoom into a module of the moon-eqms platform and explore how Documents, Tickets, CAPA, Approvals, and Workflows stay chemically bonded.
Hover to expand · Click a node to open the module
Core Modules
Five modules. One connected quality system.
moon-eqms unifies every quality process your pharmaceutical operation depends on — from controlled documents to validated workflows — in a single FDA-ready platform.
01
Document Management
Control, version, and store SOPs and regulatory documents with full audit trails to stay compliant with US FDA standards.
Explore02
Ticket Management
Create, triage, and track quality issues from report to resolution, keeping every stakeholder informed in real time.
Explore03
CAPA Management
Initiate corrective and preventive actions to address root causes and prevent recurrence of quality deviations.
Explore04
Approval Workflows
Route documents and processes through structured electronic approvals with signatures, statuses, and timestamps.
Explore05
Workflow Designer
Design, test, and deploy custom quality workflows visually to streamline operations across your organization.
ExploreBuilt for Quality
Everything pharma quality teams need, in one platform
moon-eqms unifies documents, CAPA, approvals, and workflows under a single FDA-aligned system — engineered for compliance, speed, and total traceability.
21 CFR Part 11 Aligned
Built for FDA Compliance
moon-eqms is engineered around regulatory adherence from the ground up. Every quality process is captured, controlled, and traceable so your pharmaceutical operation stays audit-ready and confidently compliant with US FDA requirements.
Audit Trails
Immutable, time-stamped records of every action across the eQMS, giving inspectors a complete, FDA-ready history on demand.
Document Versioning
Controlled revisions with full lineage and superseded-copy archiving keep your SOPs and specifications inspection-ready.
Approval Tracking
Electronic signatures and routed review chains capture who approved what and when, aligned with 21 CFR Part 11.
User Access Control
Granular, role-based permissions enforce least-privilege access so the right people reach the right quality records.
Built for every role
One platform, five quality personas
moon-eqms adapts to the people who keep pharmaceutical quality on track — from daily contributors to compliance leadership.
Drag, swipe, or use the arrows to explore each role
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Ready to Transform Your Quality Management?
Bring document control, CAPA, approvals, and audit-ready workflows together in one FDA-compliant platform. Get moon-eqms running for your team today — no credit card required to begin.
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