Vitamin K2: New Health Claims Under Review

Summary

The EFSA is reviewing 7 new health claim applications for Vitamin K2, particularly related to bone health and cardiovascular functions.

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 directly impact 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: Examine 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 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
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Conclusion

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

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Published on: 2025-08-15
Category: health-claims
Reading time: 8 minutes

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