Compliance Built Into Execution, Not Bolted On
Manufacturing compliance is not a single checkbox — it spans quality systems, regulatory traceability, asset management, supplier governance, shop floor discipline, and engineering change control. Most manufacturers cobble together separate tools for each, creating gaps, redundant data entry, and audit headaches.
The Tomax platform takes a different approach. Because every app — from EQMS to MES to EAM — shares a single data foundation and was built together from day one, compliance is embedded in your daily execution. Audit trails, traceability, CAPA workflows, and document control aren't add-ons; they're how the system works.
Whether you need IATF 16949 for your automotive OEM customers, FDA traceability for regulated products, ISO 9001 for your quality management system, or AS9100 for aerospace — the platform covers it. And with eAudit at the heart, you manage your entire audit program — internal, customer, supplier, and process audits — from one system. Load templates for any standard, capture non-conformances on the spot, assign corrective actions, and track every finding through to verified closure.
Compliance extends beyond your four walls. The Tomax platform gives you value chain visibility — from incoming material traceability through production execution to finished goods shipment — so you can demonstrate end-to-end compliance across your entire supply chain.
Start with the compliance area you need most. Expand to others without re-implementation.
Compliance Domains
Value Chain Traceability
Bolt-On Integrations
Unified Audit Trail
OEM customers are increasing audit frequency, depth, and expectations across their supply chain. If you're still preparing for audits instead of being ready for them, you're falling behind.
Weeks of preparation pulling records from multiple systems, chasing CAPA closures, and assembling evidence packages — every time a customer audit is announced.
The same non-conformances surface audit after audit because corrective actions aren't tracked to root cause closure and verified effectiveness.
Inspection records, training logs, calibration certificates, and CAPA files live in spreadsheets, shared drives, and filing cabinets — disconnected and hard to retrieve.
You can't trace compliance from your incoming materials through production to finished goods — leaving gaps that auditors find before you do.
Internal Audits That Actually Drive Improvement
IATF 16949 requires a risk-based internal audit program covering your quality management system, manufacturing processes, and products. Most manufacturers treat internal audits as a checkbox — scheduled once a year, findings logged in Excel, corrective actions that go stale.
With eAudit, your internal audit program becomes a continuous improvement engine. Schedule process audits, system audits, product audits, and layered process audits from a single calendar. Auditors capture findings on tablets or phones, assign corrective actions instantly, and track every NCR through root cause analysis, containment, and verified closure.
When a customer audit is announced, you don't prepare — you simply share access to the audit trail that's been running all along. Your internal audit results, CAPA closures, trend data, and management review minutes are already there, linked and current.
The best way to pass a customer audit is to never stop auditing yourself.
IATF 16949, ISO 9001, VDA 6.3, and custom audit templates
Risk-based audit scheduling across processes and products
Mobile audit execution with on-the-spot NCR capture
Automated corrective action assignment and escalation
Root cause analysis (5-Why, Ishikawa, 8D) linked to findings
Effectiveness verification workflows
Audit trend analytics and management review dashboards
Customer-specific requirement (CSR) tracking
Each compliance solution is powered by composable apps you can adopt independently or together.
Powered by: EQMS · eAudit · Track & Trace · Supplier Quality · Continuous Improvement
Your IATF 16949 certification depends on a living quality management system — not a set of documents that only get updated before audits. Digitize every QMS requirement so your system is always current, always traceable, and always ready for customer or certification body audits.
Customer audit readiness: evidence always current and retrievable
Internal audit program: system, process, and product audits with risk-based scheduling
Customer-specific requirements (CSR) tracking and compliance
CAPA, NCR, and 8D with root cause to verified closure
PPAP, APQP, FMEA, SPC, and Control Plan management
Value chain traceability from raw material to finished goods
Supplier audit and SCAR management with closure verification
Management review dashboards with real-time quality KPIs
Powered by: Track & Trace · EQMS · eAudit · WMS · MES
Achieve 100% unit-level traceability from raw material receipt through production to final shipment. Electronic batch records, serialization, and lot genealogy are embedded in production execution — not maintained in a parallel paper system.
100% unit-level serialization and batch genealogy
FDA DSCSA and FSMA 204 mandate compliance
Batch and lot recall management with instant impact analysis
Electronic batch records linked to production execution
Incoming, in-process, and final inspection audit trails
eAudit: schedule GMP/FDA audits, capture deviations, assign CAPA, track to closure
Powered by: EAM (ALM + CMMS + FSM) · eAudit · Asset Reliability
Maintain regulatory compliance for safety-critical assets with scheduled calibrations, inspection documentation, and complete maintenance history. Every work order, every part replacement, every inspection result is recorded and linked to the asset lifecycle.
Calibration management with automated scheduling and alerts
Regulatory inspection documentation and sign-off workflows
Safety-critical asset classification and risk-based prioritization
Maintenance compliance % dashboards (MTBF, MTTR tracking)
Warranty and certification expiry tracking
eAudit: safety and environmental audit templates with NCR capture and team assignment
Powered by: Supplier Quality · EQMS · eAudit · Track & Trace
Demonstrate that your supply chain is qualified, monitored, and governed — with incoming inspection results, SCAR closures, supplier audit findings, and delivery performance linked in a single system.
Supplier qualification and onboarding with audit-ready documentation
Supplier scorecards (quality, delivery, responsiveness, risk)
SCAR management with root cause, closure verification, and escalation
Incoming quality inspection automation with sampling plans
eAudit: schedule supplier audits, capture findings, assign corrective actions
Value chain traceability linking supplier materials to production lots and shipments
Powered by: MES · Operations Management · eAudit · Connected Worker · OEE
Digitize shop floor governance so every shift, every line, every process is audit-ready.
SOP enforcement with digital checklists and guided workflows
Operator sign-off and qualification verification
Layered process audits (LPA) with automated scheduling
Shift handover documentation
Escalation workflows with time-bound tracking
Real-time OEE and downtime categorization
eAudit for 5S, LPA, and process audits
Powered by: Manufacturing Projects · Engineer-to-Order · eAudit · MES · WMS
Control engineering changes with full impact visibility across materials, production, cost, and delivery.
Engineering Change Order (ECO) lifecycle with approval workflows
As-designed / as-built / as-maintained tracking
Impact assessment across materials, capacity, cost, and delivery
Revision control with full BOM traceability
Cross-functional change review and sign-off
eAudit configuration audits with deviation tracking
Every app reads and writes to the same data foundation. Quality events, production records, maintenance logs, and supplier data are connected — not siloed in separate systems that need reconciliation during audits.
Every action — every inspection result, every approval, every change — is automatically timestamped, attributed, and stored. You don't enable audit trails; they're always on.
Compliance evidence is generated as a by-product of daily execution — not assembled before an audit. When a customer audit is announced, you don't prepare; you simply grant access to the audit trail that's been running all along.
Trace compliance from incoming material through production to customer shipment. Demonstrate end-to-end value chain governance to auditors — not just what happens within your four walls.
Manage your entire audit program — internal, customer, supplier, and process audits — from one application. Load IATF, ISO, VDA, or custom templates. Capture NCRs on the spot. Track every finding through root cause analysis to verified closure.
Start with IATF compliance and internal audits. Expand to supplier compliance, traceability, or asset management when you're ready. Each module works independently and together — no re-implementation.
Inspection forms, CAPA workflows, approval matrices, and escalation rules are configured through the platform's no-code engine. Changes to compliance processes don't require a development project.
Real-time dashboards show compliance health across quality, maintenance, supplier, and operational KPIs. Identify risk before auditors do — not after.
Start with IATF compliance and internal audits. Expand to supplier compliance, traceability, or asset management when you're ready. Each module works independently and together — no re-implementation.
ISO 9001, IATF 16949, AS9100, VDA 6.3 — with built-in support for PPAP, APQP, FMEA, SPC, Control Plans, 8D, and closed-loop CAPA management.
FDA 21 CFR Part 11, DSCSA, FSMA 204, GMP — with electronic batch records, 100% unit-level serialization, lot genealogy, and complete chain-of-custody documentation.
ISO 55001, ISO 14001, OSHA PSM — with calibration management, safety-critical asset tracking, maintenance compliance monitoring, and environmental recordkeeping.
AS9100, CMII, ISO 9001 §8.5.6 — with engineering change order lifecycle management, BOM revision control, configuration deviation tracking, and impact assessment workflows.
The Tomax platform itself is ISO 27001 certified and SOC 2 compliant, ensuring that the system managing your compliance data meets the highest information security standards.
Whether you're preparing for an IATF certification audit, responding to FDA traceability mandates, building a world-class internal audit program, or eliminating paper-based compliance processes — the Tomax platform gives you a single, composable foundation that grows with your compliance needs across your entire value chain. Powered by composable apps from the Tomax platform. Deploy what you need today — no big-bang transformation required.