Built by a 20-year quality & operations practitioner

Walk into your next audit knowing your team will pass.

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.

Built for the standards your team actually runs
AS9100 · ISO 14001 · ISO 9001 · ITAR · NIST 800-171 · ISO 13485 · Counterfeit Parts · OSHA · EHS
QMS WORKBENCH · ONLINE
YOUR TEAM · 9:14 AM
Auditor wrote a major against Clause 8.4.3. We accepted parts from a new supplier without re-qualification. I've never written this kind of corrective action. What method do I even use?
QMS WORKBENCH
Diagnosing. This is a process control gap, not a single-event nonconformity. The right method is 5-Why followed by a CAPA with verified effectiveness, plus a Supplier Re-Qualification Procedure update. I'll run the 5-Why now and draft the corrective action.
QMS WORKBENCH
Done. Here's your artifact, ready to submit to the auditor:
PDF
Corrective Action Report: NCR-2026-038
5-WHY · CAPA · 4 PAGES · AS9100D §8.4.3
YOUR TEAM · 9:16 AM
Submitted. Auditor accepted on first review.
I've sat in your chair. I've written over a thousand findings as an auditor and closed twice that as a quality manager. The reason classroom training fails isn't the content. It's that nobody's there at 9pm when the real question shows up. We fixed that.
WT
Will Trikha
Founder · QMS Learning · 20 years
Connect on LinkedIn
Chapter 01 · The problem nobody admits

Your team passed the class. That's not the same as passing the audit.

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.

RISK 01

Findings repeat

The same nonconformity from last year's audit shows up on this year's. Your CAPAs closed without verified effectiveness. The auditor noticed.

RISK 02

Customer audits expose gaps

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.

RISK 03

The team waits for you

Every compliance question becomes your inbox. Every artifact is something you have to draft. You're the bottleneck. Capability never spreads.

RISK 04

Renewal costs compound

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.

Chapter 02 · How it works

One bundle. Three things working together.

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.

01

Online training, on their schedule

Self-paced, role-specific, built by a 20-year practitioner. No flights. No classrooms. No shop floor shutting down for three days.

What's inside AS9100D · 33 lessons
ITAR Compliance · 30 lessons
Counterfeit Parts · 31 lessons
EHS Fundamentals · 50 lessons
ISO 14001:2026 Transition · 14 lessons
Root Cause Analysis & CAPA (AS13000) · 55 lessons
ISO 9001 Internal Auditor · 35 lessons
02

An AI that picks the right method

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.

It picks from 5-Why analysis
Failure Mode & Effects (FMEA)
Corrective Action (CAPA)
Gap analysis
Root cause investigation
Risk-based change control
Supplier qualification
Internal audit prep
Nonconformity reporting
Technology Control Plans
03

A dashboard your auditor accepts

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.

Audit-Evidence Package Training records by employee
Completed scenario logs
AI-generated artifacts
Time-stamped activity
Standard-by-standard fluency
Single PDF · auditor-accepted
Chapter 03 · The unfair advantage

The AI does the diagnosis. Then it does the work.

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.

CHAT
METHOD ROUTER
DOCUMENTS
DASHBOARD
YOU TYPED:
"Same defect appeared on 3 different jobs from the same supplier this quarter."
→ Method Router selected
5-Why & Supplier CAPA
Recurring defect across multiple jobs from the same source = systemic, not isolated. 5-Why drives to root cause. CAPA closes the loop with verified effectiveness. Skip FMEA. That's for new processes, not closing existing failures.
FMEA 5-Why ✓ CAPA ✓ Fault Tree Gap Analysis
→ Artifact generated
Supplier CAPA: SUP-2026-014
5-WHY ATTACHED · 6 PAGES · AS9100D §8.4.3 · READY TO SEND
Chapter 04 · Find your team's pathway

Eight pathways. Pick the one your team needs.

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.

● Available now

Aerospace & Defense Audit-Ready

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.

AS9100D · ITAR · Counterfeit Parts
EXPLORE THIS PATHWAY →
● Available now

Commercial Aviation & Aerospace Ops

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.

RCA & CAPA (AS13000) · AS9100D · Counterfeit Parts
EXPLORE THIS PATHWAY →
● Core available, expanding

Environmental & Safety Compliance

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.

EHS Fundamentals · ISO 14001:2026 · ISO 45001 · OSHA 30
EXPLORE THIS PATHWAY →
● Pilot cohort spots open

Defense Cybersecurity Readiness

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.

CMMC · NIST 800-171 · ISO 27001 · SOC 2
EXPLORE THIS PATHWAY →
● Pilot cohort spots open

Medical Device & Life Sciences QMS

For quality leaders at medical device manufacturers. Build and audit a QMS that survives FDA inspections and ISO 13485 certification audits.

ISO 13485 · FDA 21 CFR 820 · ISO 14971 · HIPAA
EXPLORE THIS PATHWAY →
● Pilot cohort enrolling

Government Contract Accounting & DCAA Readiness

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.

CAS (48 CFR 99) · FAR Part 31 · DCAA · Incurred Cost
EXPLORE THIS PATHWAY →
● Available now

General Manufacturing Quality

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.

ISO 9001 · Internal Audit Program · CAPA · Management Review
EXPLORE THIS PATHWAY →
● Pilot cohort enrolling

Workplace Conduct & HR Compliance

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.

Harassment Prevention · EEO & Discrimination · Anti-Retaliation · Workplace Investigations
EXPLORE THIS PATHWAY →
Chapter 05 · What teams say

Quality teams who run real programs.

The root cause and corrective action training transformed how our team approaches problem-solving. We now have a structured, disciplined process across our operations.
S3 AeroDefenseAerospace & Defense
The AS9100D training exceeded our expectations. The professionalism and depth of knowledge is outstanding. They have exceeded our expectations for over 3 years.
Lowell Gwaltney Jr., CEOLG Machine
Our team is now confident in identifying hazards, conducting risk assessments, and maintaining compliance. The interactive approach made complex regulations easy to understand and apply on the shop floor.
Dave Murphy, QA ManagerCOMAV
The offer

See it in 30 minutes.

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.

Book a 30-min demo → TUE · WED · THU · 10AM–4PM PST

Document Management System

Walk into the audit with nothing left to dig for.

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.

This is the actual system, not a mockup.

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.

academy.qmslearning.com/workbench/documents
Released controlled document SOP-QC-001 with its standards mapping, segregation of duties policy, and Export Evidence Package and Download PDF actions

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.

/workbench
Drafting a Receiving Inspection Procedure in the Workbench, shown as Revision 1 draft

Drafted in plain language. Describe the procedure you need. It comes back as a controlled Rev 1 draft, ready for review and release.

/workbench/documents
Revision history showing a draft revision and a released revision, the linkage panel, and the append-only audit trail

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

Version chaos, and someone is accountable for it.

  • Three copies of the same procedure, and nobody is sure which one is live.
  • A process changed months ago. The re-training never went out.
  • Read-and-understand sign-offs scattered across email, half of them missing.
  • Evidence assembled by hand the night before, with a finding waiting for the gap you missed.

The week before an audit, with the DMS

One source of truth that answers back when the auditor asks.

  • Every document controlled, every revision kept, the current one obvious at a glance.
  • Change a document and the system flags what it touches, so nothing falls out of sync.
  • Read-and-understand acknowledgments captured and timestamped, per person, per revision.
  • The Audit-Evidence Package exports as one indexed PDF, ready to hand over.

What your team gets

Six things that turn document control into a non-event.

CONTROLLED

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.

Source of truth
REV HISTORY

An append-only trail, not a save-over

Every revision is preserved with its review and release record. The history is the evidence, and it cannot be quietly edited.

Audit-proof
ACK LOGGED

Proof your team actually read it

Read-and-understand acknowledgments captured per person and per revision, timestamped. Competence you can show, not assert.

Per person, per rev
LINKED

Tied to the standard it satisfies

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.

Clause-mapped
IMPACT

Change one thing, see what it touches

When a document changes, the system flags the linked records and training that may need to follow. Nothing drifts out of sync in silence.

Nothing left stranded
EXPORT

The binder, rebuilt in one click

The Audit-Evidence Package compiles your controlled documents, revisions, and acknowledgments into one indexed PDF, the objective evidence a registrar asks for.

Registrar-ready

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.

A consultant leaves when the invoice is paid. This stays.

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.

Book your demo 30 minutes · Tue to Thu · free 2-seat pilot for qualified teams