Coverage
Complete quality lifecycle coverage
Document control, CAPA, audits, training, change control, risk management, compliance intelligence, and dashboards — all in one platform.
Modules Hub
Modules Hub
Browse the core operating workflows that make up the Complere eQMS foundation.
Each Complere module addresses a specific quality workflow — from controlled documents and investigations to audits, training, change, and risk. Together they form a connected quality operating model that shares records, evidence, and audit trails across the entire system.
Key Benefits
How this module improves quality operations, reduces compliance risk, and supports inspection readiness for regulated teams.
Traceability
Cross-module record linking in every workflow
A CAPA can trace back to an audit finding, a document revision, a training gap, and a risk assessment — all in one view.
Adoption
Start with one module and expand from a working base
The pilot approach lets teams prove fit in one workflow before adding adjacent processes and leadership visibility.
Workflow Overview
How Complere supports the workflow
Each step in this workflow is supported by governed records, electronic signatures, and a full audit trail — so quality operations stay traceable and inspection-ready.
01
Choose your first module
Start with the quality workflow that carries your highest compliance risk — typically document control, CAPA, or audit management.
02
Configure and validate
Complere provides configuration templates and validation documentation to accelerate your first deployment.
03
Operate in governed workflows
Users work in controlled processes with electronic signatures, time-stamped audit trails, and role-based access from day one.
04
Expand into adjacent modules
Add modules progressively — linking records across systems as your quality operating model matures.
Platform Capabilities
The specific controls, features, and workflow functions built into this module to support your quality and compliance objectives.
Core Workflow
Document Control
Regulated purpose: single approved source for GxP procedures — draft through approval, effective distribution, superseded history, and retention. Authors edit with MS Office Live Edit in desktop Word, Excel, and PowerPoint, saving back as a controlled, Part 11-audited version.
Explore Document ControlCore Workflow
CAPA & Deviations
Regulated purpose: closed-loop quality events with investigation, root cause, actions, due dates, and effectiveness — traceable for audits and product release.
Explore CAPA & DeviationsCore Workflow
Audit Management
Regulated purpose: planned audits, findings, responses, and verified closure with evidence chains regulators expect.
Explore Audit ManagementLeadership & Control
Training & Competency
Regulated purpose: demonstrate personnel are qualified on current procedures — including assignments triggered by document change.
Explore Training & CompetencyLeadership & Control
Change Control
Regulated purpose: controlled assessment and release of changes to product, process, systems, and docs — with linked training and verification.
Explore Change ControlLeadership & Control
Risk Assessments
Regulated purpose: structured, ICH Q9(R1)-aligned risk evaluation linked to changes, CAPAs, and audits — so impact decisions are documented and inspection-ready.
Explore Risk AssessmentsSee every module in action during a focused demo
We tailor every demo to the modules and workflows that matter most for your quality team and regulatory environment.