DPO Radio
AesirX ComplianceOne | Manufacturing Quality & Traceability
MANUFACTURING PRODUCT QUALITY OVERLAY [ACTIVE]
Connect Product Quality, Risk Screening, Traceability, and Conformity Evidence
Prepare authority-ready manufacturing records without separating products, batches, technical rules, and corrective actions.
Why This Overlay Matters
Vietnam’s active product-quality stack combines the Law on Product and Goods Quality, Decree 37/2026/NĐ-CP, and Ministry of Industry and Trade Circulars 31, 33, and 34/2026/TT-BCT. Together they create operational work around product identification, risk classification, traceability, quality management, and conformity evidence.
The overlay is optional and manufacturing-scoped. Organizations that manufacture, import, trade, or manage affected products can install it directly after confirming scope. Other organizations can install it reference-only without activating its deadlines or score contribution.
ComplianceOne helps teams prepare, manage, and review the supporting records. It does not determine legal applicability or replace professional advice.
What The Overlay Covers
Dimension
Coverage
Scope
In-scope manufacturers, importers, product traders, supply-chain operators, and conformity or traceability owners.
Legal stack
Product and Goods Quality Law; Decree 37; Circulars 31, 33, and 34.
Product records
Product identity, category, HS code where relevant, batch/lot/serial, supplier, and responsible owner.
Quality evidence
Product-risk screening, QCVN mapping, testing, declarations, certificates, monitoring, and corrective action.
Traceability
Traceability codes, events, counterparties, locations, and supporting evidence.
Regulator-issued reference
Circular 33’s medium- and high-risk product list is treated as a reference list, not a fillable form.
How ComplianceOne Supports Manufacturing Quality Operations
Teams can maintain a structured product inventory, connect products and batches to the applicable technical rules, and retain the reasoning used for risk classification. Traceability records connect identifiers, events, parties, and evidence instead of leaving the chain across separate files.
Conformity records help track tests, declarations, certificates, coverage, validity, and renewal. When evidence fails or expires, corrective-action and recall records preserve the affected products, decisions, owners, and closure evidence.
Related Modules
Data Mapping
Compliance Forms
Structures organization-prepared product, quality, traceability, and authority-response records.
Explore Compliance Forms
Monitoring Programs
Incident Response
Audit TrailCompare the Difference
Without Structured Framework Operations
With ComplianceOne
Product, batch, supplier, and QCVN records sit in separate files.
Connect product identity, risk classification, QCVN, and conformity evidence.Risk-list screening is difficult to reproduce during review.Track traceability events against batches, parties, and supporting records.Traceability events cannot be followed as a connected chain.Route quality gaps into accountable corrective action.Expired conformity evidence is easy to miss.Reuse evidence across related manufacturing overlays without duplicating it.Built for Manufacturing Quality Operations
A product's risk classification keeps the QCVN mapping and reasoning that produced it, so a reviewer questioning why a product was screened as medium risk can see the basis rather than take the classification on faith.
Traceability events, counterparties, and locations connect to the same batch record a conformity certificate covers, so a recall investigation can follow one product's path through the supply chain instead of piecing it together from separate logs.
Expired or failed conformity evidence connects directly into corrective-action records, keeping the affected product, decision, and closure evidence together instead of losing track of what triggered the review.
See Manufacturing Quality Operations in Action
See how ComplianceOne connects product, traceability, conformity, and corrective-action evidence.
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