Collagen Manufacturer Avoids €50,000 Fine

Summary

How a collagen manufacturer was able to avoid a significant fine through timely compliance checks.

Background

This article addresses current developments in the regulation of dietary supplements. The information provided is based on official publications from EFSA, BfR, UK FSA, and other European authorities.

Key Points

• Point 1: Regulatory changes have a direct impact on your products
• Point 2: Compliance checks should be conducted regularly
• Point 3: Multi-country launches require country-specific adjustments
• Point 4: Health claims must strictly adhere to EFSA guidelines
• Point 5: Labeling requirements vary between EU member states

Practical Recommendations

For Manufacturers

1. Immediate Review: Assess your existing formulations
2. Documentation: Ensure complete compliance documentation
3. Multi-Market: Consider country-specific requirements
4. Timeline: Plan reformulations in advance

For Distributors

1. Supplier Check: Request up-to-date compliance documents
2. Product Review: Use automated tools like Supplement-Check.eu
3. Inventory: Check existing stock for compliance
4. Marketing: Adjust claims and descriptions

Compliance Check with Supplement-Check.eu

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✅ Automatic maximum levels check (BfR, EFSA, UK FSA, Swiss FSVO)
✅ Health claims validation
✅ Country-specific warnings and recommendations
✅ PDF/Excel export for your documentation
✅ AI-powered fix suggestions for non-compliance

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Conclusion

The regulatory landscape for dietary supplements in Europe is continuously evolving. Regular compliance checks are essential to avoid sales bans, warnings, and significant fines.

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Published on: 2025-01-22
Category: case-studies
Reading time: 9 minutes

Disclaimer: This article is for informational purposes only and does not constitute legal advice. For legally binding information, please consult a specialist lawyer in food law.