Manufacturing documentation
Confirm the facility and project documentation that apply to the product.
Quality, documentation and compliance considerations for UK supplement manufacturing, private label, white label and custom products.

Confirm the facility and project documentation that apply to the product.
Ensure the final specification matches the approved product brief.
Use only nutrition/health claims permitted for the product and market.
Maintain batch, best-before and quality records appropriate to the product.
Quality standards, certifications, facility scope and regulatory wording can change. Any certification or manufacturing-standard claim used for a project should be supported by current documentary evidence and should accurately describe the scope that applies to the product or facility.
If a buyer needs a specific certificate, quality document or market requirement, include it in the project brief so it can be confirmed before production.
For current Great Britain rules, use the applicable UK government and regulator guidance, including official guidance on nutrition, health claims and supplement labelling. This website does not replace regulatory or legal advice.
Clear answers for buyers, brands and trade customers planning their next supplement project.
Because certification versions, facility scope and regulatory wording can change. Only current, documented credentials should be represented as current.
Food supplements should not be marketed as treating, preventing or curing disease. Product and label claims need to comply with the rules that apply in the relevant market.
Share the product, format, quantity and brand stage. If you are not sure which manufacturing route fits, describe the outcome and we will start there.