Thirty years of pattern
recognition. Built in.

Assesses your current QMS posture against AS9100 Rev D or ISO 9001 requirements. Upload your existing documentation — or start from scratch. AI evaluates compliance posture clause by clause, identifies gaps, and produces a prioritized remediation list with effort estimates. Designed to answer the question every shop owner asks first: "Where do I actually stand?"

Root cause analysis is an input to a corrective action record — not a separate activity. This tool combines both into a single workflow structured around the 3-Legged 5-Why methodology used in aerospace. AI validates root-cause logic, identifies gaps in the why chain, and flags when a proposed cause doesn't connect to the nonconformance. Produces documentation suitable for customer or registrar submission.

Upload your QMS documentation. AI identifies risk points specific to your organization and generates company-specific audit questions tailored to your actual processes — not generic checklist items. Findings are entered during the audit, categorized by clause and severity, and a formal audit report is produced. The output is what you hand to your registrar.

Parses purchase order requirements — special processes, first article requirements, certifications, test requirements, traceability — and flows them down to the work order level. AI identifies requirements that are easy to miss under production pressure. Catches the missed PO requirements that generate customer complaints and failed audits. Touches every order, every time.

Tracks personnel training requirements, completion status, and competency records across your workforce. Structured workflow tool — purpose-built logic, no AI in runtime because none is needed. Captures training events quickly, maintains a complete history, and surfaces gaps before an auditor does. Produces a training matrix that satisfies registrar evidence requirements.

Manages calibration schedules, records, and out-of-tolerance events for all measurement and test equipment. No more missed deadlines, no more scrambled pre-audit searches. Structured workflow — the logic is straightforward and doesn't need AI. Produces a calibration register that satisfies AS9100 Clause 7.1.5 evidence requirements exactly.

Complete document lifecycle management — revision control, approval workflows, distribution records, and obsolescence control. The backbone of any auditable QMS. Structured workflow tool built around what Clause 7.5 actually requires. Controls the documented information that defines your quality system without the administrative burden of managing it manually.