Online compliance training for your quality, EHS, and compliance team. Plus an AI assistant that diagnoses the problem, picks the right method, and produces the document your auditor accepts.
When your team hits a problem they haven't seen before. An unexpected nonconformity. A supplier change that might trigger Clause 6.3. A finding they don't know how to close. They freeze. The AI picks the tool. 5-Why. FMEA. CAPA. Gap analysis. Root cause. Then it writes the artifact for them. They stop guessing. They start delivering.
The certificate goes on the wall. Six months later the auditor walks in. The team that "completed training" can't tell her which of the 23 control families NIST 800-171 covers. Can't write a nonconformity statement with objective evidence. Can't decide whether a supplier change triggers Clause 6.3. They freeze. The findings stack up. The CEO asks why.
The same nonconformity from last year's audit shows up on this year's. Your CAPAs closed without verified effectiveness. The auditor noticed.
Your Tier 1 customer's audit team asks your shop floor what process X looks like. The answer doesn't match the SOP. The contract goes on hold.
Every compliance question becomes your inbox. Every artifact is something you have to draft. You're the bottleneck. Capability never spreads.
Annual classroom retraining at $1,500 per seat plus travel. Same gap, same scramble, same line item your CFO highlights every budget cycle.
Training is what you buy. Capability is what you actually need. They're not the same thing.
Online training builds the foundation. The AI handles the live questions. The Manager Dashboard turns it into evidence the auditor accepts. One product. One bundle. One PDF you walk into the audit room with.
Self-paced, role-specific, built by a 20-year practitioner. No flights. No classrooms. No shop floor shutting down for three days.
When your team hits a real problem, the AI diagnoses what it actually is. Process gap. Isolated incident. Supplier change. Design issue. Then it picks the method that fits (5-Why, FMEA, CAPA, gap analysis, root cause) and writes the artifact in your standard's voice.
See who's competent on what. Where the capability gaps are. What the team has produced. Export one PDF that contains training records, completed scenarios, generated artifacts, and time-stamped activity. A registrar accepts it as objective evidence of training effectiveness.
Generic AI gives you generic answers. This one was trained on real audits, real findings, and 20 years of figuring out which compliance method to apply when. It diagnoses the problem first, picks the method second, writes the artifact third. Your team stops freezing.
Most quality professionals know what 5-Why, FMEA, and CAPA are. The hard part isn't the methods. It's knowing which one to reach for when a problem walks in the door at 9am Monday and the auditor's coming Friday.
That decision, which method fits this problem, is the gap. It's why senior quality people are valuable. It's also why everyone else freezes.
The AI is trained on the diagnosis, not just the methods. Show it the problem in plain English. It tells you which method fits. Then it does the work. Your junior quality engineer becomes useful on day one.
Each pathway is a bundle of courses, the AI assistant scoped to your standards, and a Manager Dashboard mapped to your audit calendar. We customize the rollout in the demo.
For QMS managers running AS9100 across single or multi-site operations. Walk into every AS9100, ITAR, and counterfeit parts audit with answers, evidence, and a Manager Dashboard your auditor accepts.
For EHS managers carrying both environmental and safety obligations. Handle ISO 14001:2026 transitions, OSHA inspections, and incident investigations without the panic call to a consultant.
For defense contractors facing CMMC deadlines and the loss of contracts if they miss them. Build the SSP, close the POA&M gaps, walk into the C3PAO assessment prepared.
For quality leaders at medical device manufacturers. Build and audit a QMS that survives FDA inspections and ISO 13485 certification audits.
For quality leaders at manufacturers running ISO 9001 across single or multi-site operations. Run internal audits, manage CAPA, execute management review the same way at every plant.
Pick the two people on your team who'd benefit most. Give them 14 days inside the platform. Watch them stop freezing on the questions they used to escalate to you. If the fit's not there, walk away. No credit card. No follow-up calls. No obligation.