Biozid-Produkte 2026: Sind Sie konform?

Are you prepared for ongoing BPR requirements?

Avoid fines of up to €50,000 per violation and authorization issues!

The Biocidal Products Regulation (BPR, (EU) 528/2012) requires continuous updates, including new active substance approvals (e.g., via delegated acts like (EU) 2025/1490), integration of CLP updates (new hazard classes such as ED/PBT), and recommended digital elements like QR codes for e-SDS (source: ECHA/BAuA). Stricter sustainability assessments (e.g., environmental compatibility) apply to both substances and products. Many SMEs overlook minor errors in labels, SDS, or authorizations, which can result in fines, product recalls, or market restrictions.

The tough reality for SMEs:

• Complex requirements: Errors in authorization numbers, CLP classification, or claims can lead to significant fines.

• Stricter audits by customers and authorities: Missing exposure scenarios or national rules (e.g., TRGS 512 in Germany) may result in delivery stops.

• Common pitfalls:Outdated substance evaluations, missing UFI codes, or incomplete multilingual labeling.

Have we sparked your interest?
Then we look forward to hearing from you.