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1factory eQMS Ties Shop-Floor Inspection to CAPA and Audit Readiness

1factory eQMS Ties Shop-Floor Inspection to CAPA and Audit Readiness

1factory formally introduced its electronic quality management system (eQMS) in a September 11, 2026 press release—ASSEMBLY Magazine covered it September 29—to close the split between compliance binders and shop-floor inspection. Document control, training, CAPAs, SCARs, complaints, and audit readiness sit in one cloud platform natively tied to the company’s inspection and supplier quality tools already used on the floor.

That is the daily QMS fight: auditors ask how procedures connect to measurement data and nonconformances, and plants answer with days of scramble. Connecting compliance execution to MES inspection reality—and keeping change and product context visible through PLM—is the bar, not another standalone document vault.

Dimensional metrology technician calibrating a boresight collimator in a calibration lab—audit-ready measurement discipline. U.S. Navy photo by Greg Vojtko.
Audit readiness is continuous calibration and linked records, not a binder build the week before the auditor arrives. U.S. Navy photo by Greg Vojtko (Wikimedia Commons).

“Quality leaders tell us the same problems over and over: they don’t want another disconnected system, and they don’t want to spend a year implementing one,” said Michael Corrales, VP Manufacturing Solutions at 1factory. “The 1factory eQMS goes live in days, not months… and it connects compliance directly to what’s happening on the shop floor.” Customer VIDAR (an ITT company) cut audit preparation 83%—from three days to four hours—after replacing a fragmented paper quality system.

The platform targets ISO 9001, AS9100, ISO 13485, and IATF 16949. 1factory will demo at the Assembly / Quality Show October 27–29 in Rosemont; Quality Digest also flagged IMTS and FABTECH demos around the same launch window. Courses now manage external safety and certification training with the same version control as internal procedures.

Dial test indicator checking runout on a lathe cross-slide—shop-floor inspection that must feed CAPA and complaints. Photo: David English / Wikimedia Commons.
Shop-floor measurements only protect the plant when they feed CAPA, SCAR, and complaint loops in the same system of record. Photo: David English (Wikimedia Commons).

Secondary context, same thesis: FDA’s Quality Management System Regulation (QMSR) is now in effect, and inspections on or after February 2, 2026 moved off the old QSIT checklist model toward how the quality system operates in practice—linked CAPA, complaints, supplier oversight, risk, and training—not isolated binders (QT9 / European Pharmaceutical Manufacturer, Oct. 1, 2026).

For N23D, the job is plain English: document control, training, CAPA/SCAR, complaints, and audit readiness belong in one native Rust binary with MES inspection and PLM product context—a real QMS surface, not compliance theater next to the floor.

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