Quality Management (eQMS)
Deviation, CAPA, complaint, and change control — all in one place. Configurable to your actual SOPs, not a fixed template someone else designed. Electronic signatures and 21 CFR Part 11 alignment from day one, not bolted on later.
What's Inside the eQMS Module
Everything your quality team runs on, minus the 12-month implementation and the features you'll never use.
Deviation Management
Raise, investigate, and close deviations with structured workflows. Each deviation links to affected batches, equipment, and SOPs automatically — no manual cross-referencing.
CAPA Tracking
Go beyond logging. AI-assisted root cause suggestions, effectiveness checks, and escalation workflows that keep CAPAs from sitting open for months.
Complaint Handling
Capture customer complaints, link them to production data, and manage investigations through resolution. Trending built in so you catch patterns early.
Change Control
Manage planned changes to processes, equipment, materials, and SOPs. Impact assessment, approval routing, and implementation tracking — all connected to the rest of your quality data.
Electronic Signatures
21 CFR Part 11 and EU Annex 11 compliant e-signatures built into every workflow. Meaning and intent captured with every signature — no separate signature module to buy.
Configurable Workflows
Map the system to how your plant actually runs. Your SOP numbering, your approval chains, your escalation rules — not a template from a company with different processes.
Your Quality System Should Work Like Your Plant Does
See how the eQMS module maps to your actual SOPs and workflows — not the other way around.