---
title: Can you manage Substances of Concern for Packaging?
description: SyncForce supports the management of substances of concern within the Packaging Specification Manager
---

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# Can you manage Substances of Concern for Packaging?

## SyncForce supports the management of substances of concern within the Packaging Specification Manager.

By giving packaging teams one place to capture, review and monitor compliance-relevant data for heavy metals limits, PFAS restrictions and SVHC presence at Packaging Assembly Unit ([PAU](https://support.syncforce.com/knowledge/codes-and-abbreviations-a-to-z?hsLang=en)) level.

This fits well with the direction of the EU **Packaging and Packaging Waste Regulation (PPWR)**, which entered into force on 11 February 2025 and generally applies from 12 August 2026, and which sets requirements for the composition of packaging placed on the EU market.

For **heavy metals**, SyncForce allows users to register whether the limit applies, whether a glass derogation is relevant, whether values are below the limit of detection, and to record the **total heavy metals** result. This helps teams document restricted-substance checks in a structured and auditable way based on declarations or test evidence.

For **PFAS**, SyncForce supports both screening-based and direct-result workflows. Users can record whether PFAS restriction applies, whether PFAS were intentionally added, the **assessment entry route**, and the relevant outcomes such as **total fluorine**, **organic fluorine**, **Any PFAS**, **Sum PFAS**, and **Total PFAS including polymeric PFAS**. This enables a practical compliance workflow where businesses can distinguish between initial screening, direct laboratory results and final compliance assessment.

For **SVHC presence**, SyncForce supports declaration and evidence handling for Candidate List substances. Users can record the **declaration status**, whether an SVHC is **present above 0.1% w/w**, the **Article 33 communication status**, and the **SCIP status**. When an SVHC is present, individual substances can be registered with identifiers such as **CAS number**, **EC number**, concentration and converted **mg/kg** value. This helps companies manage both internal assessment and downstream communication obligations linked to packaging substances of concern.

In practice, this means SyncForce does not just store a yes/no compliance answer. It supports the full process of **evidence collection, data entry, review, exception handling, communication status and traceable decision-making** for packaging compliance. That makes it a strong foundation for PPWR-related packaging data management, especially where manufacturers need to combine supplier declarations, test data and regulatory follow-up in one controlled workflow.

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