Vitamin D: Demand Surge in Winter 2025

Summary

Vitamin D demand increased by 45% in autumn 2025. How manufacturers can secure the supply chain.

Background

This article addresses current developments in the field of dietary supplement regulation. 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: Check your existing formulations
2. Documentation: Ensure complete compliance documentation
3. Multi-Market: Account for country-specific requirements
4. Timeline: Schedule reformulations in a timely manner

For Retailers

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

With Supplement-Check.eu, you can verify your products' compliance across all 28 EU+UK+CH markets in just minutes:

✅ 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 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 hefty fines.

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Published on: 2025-10-20
Category: case-studies
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.