Send a short brief and DAT will route it to the right working track — white-label, semi-custom or custom development. Reviewed by the manufacturing team, not an autoresponder.
Pick a reviewed gummy concept from the catalogue and adapt brand artwork. Fastest path to a launch — packaging, claims and documentation reviewed against the target market.
Use this route in the brief →Adjust dose, flavour or active stack within an existing matrix. Differentiated SKU without a full custom-development cycle.
Use this route in the brief →Bespoke formulation, custom flavour profile and packaging dieline. The right route for category-defining launches with longer planning windows.
Use this route in the brief →Project briefs are handled in the DAT portal. The wizard prompts for the inputs below — the more upfront context, the faster DAT can confirm feasibility and the right working route.
Primary distribution market and any secondary markets — drives label, claims and notification scope.
Indicative MOQ tier and forecast for the launch window. Used to confirm route and packaging.
Positioning, active ingredients in scope and any non-starters. Custom development is reviewed against the brief.
PET bottle, doypack or sachet — pack format influences the production route and documentation set.
Target launch window. Production calendar and raw-material lead times are confirmed in the quote.
Any approved claim wording, regulatory framework, or label requirement you already need to honour.
Required fields are marked with an asterisk. Everything else helps the manufacturing team route the brief faster.
Once your brief is received, DAT will reply with the right next step and (if the brief fits) deep-link the project into the portal workspace. Inside the portal the project moves through brief review, formula and spec confirmation, artwork and label review, production and QC, and batch-specific document release.
These guides cover the regulatory framework, claim review process and project timeline for private-label gummy launches.
DAT Supply manufactures food supplements only. On-pack health and nutrition claims must comply with EU Regulation 1924/2006 and the authorised list under EU 432/2012. Claim wording is reviewed per project. The brand owner remains the food business operator and is responsible for final filings in each target market. Documentation availability depends on product, market, and project stage.