Platform

One Quality Platform. One Connected Workflow.

Four layers. The boundaries between them are where quality work usually leaks — re-typed characteristics, documents that disagree, evidence collected by hand. Here they are the same system.

The hand-offs

The connections are the product.

Any vendor can list modules. What matters is what each one hands to the next, because that hand-off is the work your team currently does by retyping. Select a stage.

Every module

What is in the platform today

Everything listed here exists in the product now. Roadmap items are on the homepage, clearly marked as roadmap.

PL

Product lifecycle

What a part goes through once, from first drawing to approved submission.

Parts

The part record: number, revision, customer, drawing, and the characteristics taken from it. This is the single source every later document references.

APQP

Projects with phases and activities, owners, due dates, approvals and the documents each activity produced.

PPAP

Submission elements set by the customer’s requirement profile, with evidence linked to the records that satisfy them.

RP

Risk & process

What could go wrong, and what is done about it.

FMEA

DFMEA and PFMEA in AIAG-VDA structure — failure modes, effects, causes, prevention and detection controls, risk evaluation and actions — with revisions and a Draft → Review → Released workflow.

Process

The operation sequence and which characteristics each operation makes or verifies. The spine both the PFMEA and control plan are built on.

Control Plan

What is measured at each operation, to what specification, with which gauge, how often, and what happens on a failure.

QE

Quality execution

Measured reality, and what it says about the process.

Inspection

Results against specification, with the gauge used and its calibration state, recorded per characteristic.

SPC

X̄–R control charts with calculated limits, Nelson rules for out-of-control signals, and Cp / Cpk / Pp / Ppk.

GV

Governance

What makes the records above hold up.

Quality

Nonconformances, 8D investigations and corrective actions, linked to the part and the process.

People & Gauges

Who is qualified for which work, and which gauge is in calibration — both of which an inspection result depends on.

Customer

The customer record every submission, requirement and profile hangs from.

Customer Requirements

What one specific customer asks for, held against that customer rather than in a shared folder.

Requirement Profiles

A reusable rule set per customer: required elements, naming, sequence, approval roles, submission rules.

Approval Routes

Who approves what, in which order, before a document can be released.

Documents

Controlled documents with revision, version, owner, state, effective date and change reason.

Form Templates

The output format a customer expects, produced from the structured record.

Get started

Ready to simplify your quality workflow?

Bring APQP, FMEA, PPAP, process flow, control plans, inspection and SPC into one connected platform.

Questions? support@easyqualityflow.com