Reviewed concept, brand artwork
Pick a reviewed gummy concept from the public catalogue and adapt brand artwork. The fastest path to a launch — packaging, claims and documentation are reviewed against the target market.
Manufacturing
Gummies-first manufacturing for private-label supplement brands.
One product category, three working routes, and a documentation flow gated by project stage. The brand owner remains the food business operator on pack.
Gummies first
One category, taken seriously.
DAT manufactures pectin-based gummy supplements. We do not split attention across powders, capsules or RTD formats. The discipline is narrow on purpose — depth of formulation, packaging and documentation review, not breadth of categories.
Working routes
Three working routes
Every project fits one of these routes. The route shapes the documentation set and the project timeline; final routing is confirmed inside the portal.
Adjusted within an existing matrix
Adjust dose, flavour or active stack within an existing matrix. Useful for differentiated SKUs without a full custom-development cycle.
Bespoke formulation, custom dieline
Fully bespoke formulation, custom flavour profile and packaging dieline. The right route for category-defining launches with longer planning windows.
Format axis
PET bottle · Doypack · Sachet
Format is independent from positioning. The same formula concept can move across packaging types — DAT confirms the right fit during the brief.
- Bottle
Bottle gummies
Best for classic white-label gummy launches: PET / HDPE bottle, retail-friendly, broad market fit.
Format is confirmed per project — DAT reviews packaging, fill, outer carton and logistics against the brand brief before specification.
- Doypack
Doypack gummies
Lighter, flexible packaging for premium retail concepts and DTC ranges with smaller footprint.
Format is confirmed per project — DAT reviews packaging, fill, outer carton and logistics against the brand brief before specification.
- Sachet Premium daily-use
Sachet gummy concepts
Routine-based, travel-friendly, premium daily-use formats. Sachet configuration is confirmed per project, including gummies per sachet, sachets per unit, film, outer packaging and logistics.
Format is confirmed per project — DAT reviews packaging, fill, outer carton and logistics against the brand brief before specification.
Production process
Brief to released batch
Each step is reviewed before the next gate opens. The Certificate of Analysis is batch-specific and post-production after QC release.
- 01
Brief review
Target market, format, quantity, claims direction.
- 02
Route
White-label, semi-custom or custom — confirmed against the brief.
- 03
Spec lock
Per-SKU specification + allergen statement drafted, then locked.
- 04
Artwork
Dieline + on-pack copy reviewed against the target-market framework.
- 05
Production & QC
In-process control plan agreed; production runs through the controlled network.
- 06
Batch release
Batch-specific COA after QC release; documentation refreshed per stage.
Documentation route
Project gates, not promises
DAT releases documentation as the project moves through each gate. The Certificate of Analysis is batch-specific and always issued post-production after QC release.
Gate
Stage
Reviewed
When
Brand owner receives
- 01StageBrief reviewReviewed
Target market, format, quantity, claims direction
WhenProject entry
ReceivesFeasibility view + working route confirmation
- 02StageFormula & spec confirmationReviewed
Formulation route, allergen statement, per-SKU specification
WhenAfter brief sign-off
ReceivesSpecification draft + spec-locked formula
- 03StageArtwork & label reviewReviewed
Dieline, on-pack copy, claim wording per market framework
WhenIn parallel with spec lock
ReceivesReviewed artwork against the target-market framework
- 04StageProduction & QCReviewed
In-process control plan, stability and QC release rules
WhenOnce spec & artwork are signed off
ReceivesProduction run + in-process control records
- 05StageBatch-specific documentsReviewed
Per-batch QC, traceability, release-for-shipment
WhenAfter production & QC release
ReceivesBatch-specific Certificate of Analysis + traceability
- 06StageRepeat order supportReviewed
Forecast review, raw-material lead times, improvement notes
WhenPer repeat order
ReceivesRefreshed documentation per project stage
Documentation availability depends on product, market and project stage. The brand owner remains the food business operator and is responsible for final filings in each target market.
Brief inputs
What DAT needs before reviewing manufacturing
The inputs below shape the route, the format, the documentation set and the project timeline.
- 01 Target market
Primary distribution market and any secondary markets — drives label, claims and notification scope.
- 02 Quantity
Indicative MOQ tier and forecast for the launch window. Used to confirm route and packaging.
- 03 Formula direction
Positioning, active ingredients in scope and any non-starters. Custom development is reviewed against the brief.
- 04 Packaging format
PET bottle, doypack or sachet — pack format influences the production route and documentation set.
- 05 Timeline
Target launch window. Production calendar and raw-material lead times are confirmed in the quote.
- 06 Claims & label requirements
Any approved claim wording, regulatory framework, or label requirement you already need to honour.
Launch resources
Practical guides for your project
Controlled disclosure
Approved production network, controlled by project stage
DAT operates an approved production network and a controlled disclosure model. Supplier identity, factory references and full technical documentation are released to brand owners by project stage and disclosure need — never as a public list. This protects both the brand and the production partners we work with.
- Controlled manufacturing route, confirmed per project
- Project-stage documentation; batch-specific QC release
- Target-market review for claims, labelling and notifications
A note on claims and compliance
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.
Project handoff
Start a manufacturing project
Send your project brief — DAT will review and route it to the right working track. Final routing is confirmed inside the portal once the brief has been reviewed.