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Complere.tech
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Complere is a validation-ready eQMS for regulated life-sciences teams โ pharma, biotech, medical device, diagnostics labs and CDMOs. It connects your quality records, actions, people and evidence into one operating system, so quality and compliance run on a single shared audit trail and permission model instead of scattered spreadsheets, email and disconnected tools.
Eight quality modules, one connected system: ...Document Control ...CAPA ...Events/Deviations ...Training & Competency ...Audit Management ...Change Control ...Risk Assessments (ICH Q9 / ISO 14971) ...Supplier Management These are linked end to end for traceability from a requirement to a record to its evidence.
Compliance is built in, never an upsell: Every plan ships with both validation approaches the FDA recognises โ CSV (VMP, URS, IQ/OQ/PQ, traceability) and the risk-based CSA pack โ at no extra cost, plus 21 CFR Part 11 e-signatures, immutable ALCOA+ audit trails, EU GMP Annex 11 alignment, ISO 13485 record-keeping and GAMP 5 methodology. Role-based access, MFA and SSO are standard.
A built-in Compliance Intelligence layer: Get a real-time view of compliance health: a Compliance Cockpit scoring every module, an Obligation Registry mapping regulations to controls and evidence, a one-click Inspection Pack (signed, hashed, reproducible), a CSA Evidence Graph, an Executive Compliance Index, and an explainability panel behind every score โ so leaders and auditors always see why.
Built for how regulated teams actually work: Start free with a Pilot in a validated environment, prove value on one workflow, then expand. Where many enterprise rollouts take 6โ12 months to the first controlled record, Complere gets you live in days to weeks โ with the validation pack (a $25โ50K value elsewhere) included.
Audit-ready, explainable and inspection-ready by design.
Start free โ https://complere.tech/pricing
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Complere.tech's answer:
Design-partner pharma, biotech and medtech teams (names under NDA)
Complere.tech's answer:
Regulated life-sciences organisations โ pharmaceutical, biotech, medical device, diagnostics/CLIA labs, CDMOs/CMOs and nutraceuticals โ operating under GxP and data-integrity rules. Users include Heads/VPs of Quality, QA managers and site quality leads, regulatory and compliance officers, validation/CSV and document-control teams, training and CAPA/audit owners, and quality executives, from emerging SMBs to multi-site enterprises.
Complere.tech's answer:
A modern web stack: Laravel (PHP) on the backend and Nuxt 3 / Vue.js on the frontend, delivered as a multi-tenant cloud SaaS on AWS with per-tenant data isolation. Quality is engineered in, not bolted on: backend unit and feature tests run on PHPUnit (Laravel's testing framework, with Pest), and end-to-end automation runs on Playwright. A CI/CD pipeline drives touchless deployment โ every release automatically executes the unit and automation suites and regenerates validation and CSA assurance evidence (JUnit/Allure reports serving as OQ evidence), so validation is continuous rather than a one-off project. REST API plus webhooks for integrations; SSO (SAML/OIDC, Azure Entra) and MFA for access.
Complere.tech's answer:
Complere unifies all eight quality modules on one shared audit trail, permission model and validation posture - and ships both FDA-recognised validation approaches (CSV and CSA) in every plan at no extra cost, where competitors charge $25โ50K separately. Its standout is a built-in Compliance Intelligence layer: a live compliance score per module, an obligation-to-evidence map, a one-click signed Inspection Pack, and an explainability panel behind every number - so quality is real-time and inspection-ready, not reconstructed from spreadsheets.
Complere.tech's answer:
You pay for the plan you run, not a 12-module enterprise SKU. Validation is included (not a separate fee or a partner project), you start free with a real Pilot in a validated environment, and most teams are live in days to weeks versus the 6โ12 months typical of legacy suites. You get enterprise-grade compliance โ 21 CFR Part 11 e-signatures, immutable ALCOA+ audit trails, EU GMP Annex 11, ISO 13485, GAMP 5 โ without enterprise-grade complexity or cost. And it's built by a team with 30+ years of collective quality-management experience, so the workflows reflect how regulated teams actually operate. Typically 30โ60% lower Year-1 TCO than Veeva, MasterControl, ETQ or Sparta.
Complere.tech's answer:
Complere began with a pattern its founders kept seeing from inside the audit room. Across inspections and supplier audits, they watched capable quality teams scramble โ reconstructing evidence from spreadsheets and email, chasing signatures, and proving traceability after the fact โ while the eQMS platforms meant to help cost six figures and took months before capturing a single controlled record.
Drawing on 30+ years of collective quality-management experience, they set out to build the system they wished they'd had: validation-ready on day one (CSV and CSA included), explainable enough to defend live in front of an inspector, and affordable enough for growing companies. The result is Complere โ an eQMS where compliance is never an upsell, and where quality teams walk into audits calm instead of firefighting.
