One live revision, never a wrong copy
The current document is the one your team sees. Superseded revisions are kept, but they cannot be mistaken for live.
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 distributors, MROs, repair stations, Tier 1 suppliers, and aerospace operations. Build the RCA discipline that closes customer findings on first submission. Train your team on AS13000 8D, 5-Why, FMEA, and CAPA effectiveness verification your customer or registrar 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 controllers, CFOs, and DCAA-compliance leads at defense contractors. Know whether CAS applies and at what level, defend every allocation, and stay ahead of the 2026 threshold and GAAP-conformance changes rewriting the framework. Built for the finance org, not the quality org.
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.
For HR and operations leaders who have to prove training actually happened when a charge lands. State-mandated harassment and discrimination training your whole workforce finishes, with completion records that hold up as a legal defense.
We walk you through a Workbench session, show the manager dashboard, and demo the audit-evidence PDF export end to end. After the demo you'll know exactly how this fits your team and where pricing lands.
Document Management System
The auditor asks for a procedure. You do not open a shared drive and hope it is the current revision, and you do not chase sign-offs that were never logged. Every controlled document lives in one place, every revision kept, every acknowledgment on record. When the auditor wants proof, you hand it over in one click. In a regulated shop that is not convenience. It is the certification your contracts depend on, protected.
30 minutes · Tuesday to Thursday · free 2-seat pilot for qualified teams
The cost
70 to 90% less than classroom
No travel, no seats sitting empty on the floor, no per-head classroom invoice. The capability stays in house.
The speed
Audit evidence in minutes, not days
Controlled documents, revisions, and acknowledgments compile into one indexed package on demand.
The risk
A major finding puts the cert at risk
In aerospace and defense, the certification is what lets you bid. Loose document control is where findings start.
A controlled document that knows the standards it satisfies, the revisions behind it, and the records it links to. No binders. No guessing which one is live.
Released and mapped. The current revision, every standard it satisfies, and the Audit-Evidence Package one click away. This is the controlled record, not a file in a folder.
Drafted in plain language. Describe the procedure you need. It comes back as a controlled Rev 1 draft, ready for review and release.
Every revision and action, on the record. Draft, review, release, with an append-only audit trail and links to the clause, corrective action, related document, or training record.
The week before an audit, today
The week before an audit, with the DMS
What your team gets
The current document is the one your team sees. Superseded revisions are kept, but they cannot be mistaken for live.
Every revision is preserved with its review and release record. The history is the evidence, and it cannot be quietly edited.
Read-and-understand acknowledgments captured per person and per revision, timestamped. Competence you can show, not assert.
Documents link to the clause, the training, and the related records they support, so coverage is visible and gaps surface before an auditor finds them.
When a document changes, the system flags the linked records and training that may need to follow. Nothing drifts out of sync in silence.
The Audit-Evidence Package compiles your controlled documents, revisions, and acknowledgments into one indexed PDF, the objective evidence a registrar asks for.
Built by a practitioner, not an academic. Two decades inside AS9100 and ITAR audits shaped how every revision, linkage, and acknowledgment works. This is document control the way someone who has sat across from the auditor would build it.
Your living QMS lives in the system your team uses every day. The capability does not walk out the door, and your controlled document history is yours to keep.