Curcumin Formulations: Bioavailability & Claims

Summary

Which curcumin formulations are permitted, and which health claims can be used? An overview.

Background

This article addresses recent 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 across EU member states

Practical Recommendations

For Manufacturers

1. Immediate Review: Examine your existing formulations
2. Documentation: Ensure complete compliance documentation
3. Multi-Market: Take country-specific requirements into account
4. Timeline: Plan reformulations well 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 accordingly

Compliance Check with Supplement-Check.eu

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

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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 hefty fines.

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Published on: 2025-05-22
Category: health-claims
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.