Packaging machinery answers to a fast-moving compliance landscape, Machinery Regulation (EU) 2023/1230, the Packaging and Packaging Waste Regulation (PPWR) 2025/40, ANSI/PMMI B155.1 and EN 415 among them. Govern & Trace for PM equips your engineering teams to prove that landscape is met, with records that connect format to recipe, label to product, and every line back to its compliance evidence.
Govern & Trace for PM brings together format governance, label traceability, serialization systems, compliance records and connected packaging data, the record-keeping that keeps a high-SKU packaging operation accurate and auditable. Format governance and label traceability keep formats, recipes and labeling correct for every SKU and customer configuration, while serialization systems give every unit, case and pallet a verifiable identity through the supply chain. Compliance records consolidate the safety and conformity documentation your line needs for acceptance and audit, and connected packaging data closes the loop, turning machine performance into evidence you can act on.
The result: a defensible, audit-ready record for every format, label and line you run, ready whenever a customer, auditor or regulator asks for it.
Implement serialization for traceable, auditable packaging
Serialization Systems enable package‑level identity, aggregation and parent‑child traceability so each unit, case and pallet is verifiable through the supply chain. This is essential for pharma, medical devices, regulated goods and high‑value products where serialization prevents counterfeits, supports recalls and fulfils regulatory obligations.
We integrate camera verification, code grading, reject confirmation, aggregation stations and site‑server interfaces with line controllers and enterprise systems so serialization is reliable, auditable and operationally practical across the packaging line.
Design unit, bundle, case and pallet‑level serialization structures.
Define parent‑child data models and aggregation workflows.
Integrate camera checks, code grading, reject confirmation and rework flows.
Plan line‑controller and site‑server interfaces for data capture and exchange.
Map data exchange using GS1 identifiers where applicable for interoperability.
Provide audit trails and electronic record requirements for compliance.
Prepare DSCSA readiness and serialization inputs for prescription‑drug packaging.
Pharma Packaging | Medical Products | Market-regulated Nutraceuticals | High-Value Consumer Goods | Export Packaging | Anti-Counterfeit Packaging.