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DAT Supply Nutraceutical manufacturing
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Manufacturing

Private-label supplement manufacturing across the formats brand owners actually launch.

One manufacturing network, three working routes, four documentation gates — applied across gummies, soft chews, oral strips, capsules, softgels and adjacent formats. The brand owner remains the food business operator on pack.

Start your project Market guides
DAT Supply private-label manufacturing
Format pages
12

reviewed format money pages live.

Working routes
3

white-label, semi-custom, custom.

Project gates
4

brief · spec · artwork · release.

Pathways
EU · UK · US

reviewed per target-market framework.

Manufacturing platform

One platform, taken seriously across formats. Depth of formulation, packaging and documentation review — not a marketplace of vendors.

DAT manufactures private-label nutraceuticals through a project-managed production workflow. Format is chosen against the brand brief — not the other way around.

Formats

Private-label formats reviewed end to end

Each format runs through the same four-gate model — brief, spec, artwork, release — so the documentation set, packaging and positioning stay aligned across the range.

  1. Gummies

    Pectin-based supplement gummies — the mature DAT Supply format. Used across daily wellness, beauty, sleep and kids ranges.

    Private label gummies →

  2. Filled gummies

    Gummies with a liquid or paste-filled centre. Advanced sub-format; reviewed per project against the brief.

    Private label filled gummies →

  3. Soft chews

    Soft, paste-based chewable supplement format. Distinct from gummies — its own matrix, base and process.

    Private label soft chews →

  4. Capsules

    Hard or vegetarian capsule format. Reviewed per project; documentation route follows the standard project gates.

    Private label capsules →

  5. Softgels

    Softgel format for oil-soluble actives. Reviewed per project; sub-supplier capability confirmed during the brief.

    Private label softgels →

  6. Tablets

    Compressed tablet format. Reviewed per project; finish (uncoated, film-coated, chewable) confirmed during the brief.

    Private label tablets →

  7. Powders

    Loose powder or scoopable supplement format. Format confirmed per project — jar, doypack, sachet or tub.

    Private label powders →

  8. Liquid drops

    Dropper-bottle supplement format for oil-soluble or precise-dose actives.

    Private label liquid drops →

  9. Shot vials

    Single-serving liquid shot vial format. Reviewed per project against retail and logistics constraints.

    Private label shot vials →

  10. Oral strips

    Fast-dissolving oral strip format. Reviewed per project; payload range confirmed during the brief.

    Private label oral strips →

  11. Functional jellies

    Pouchable functional jelly format for daily-routine and on-the-go supplement concepts.

    Private label functional jellies →

  12. Functional snacks

    Snack-style functional formats. Concept review during the brief — DAT confirms feasibility before quoting.

    Private label functional snacks →

  13. Pet supplements

    Soft chews and adjacent formats for dog and cat wellness ranges, reviewed per species claim framework.

    Private-label pet supplements →

Launch routes

Pick the route that matches the brief.

Every project moves through one of three routes. Final routing is confirmed inside the portal — the route shapes the documentation set and the timeline.

01 · White-label

Reviewed concept, brand artwork.

Pick a reviewed pectin-gummy concept from the catalogue and adapt brand artwork. The fastest path from brief to launch — packaging, claims and documentation are reviewed against the target market.

Best for
First gummy SKU · short timelines
Lead time
Confirmed in the quote
Start with this route 02 · Semi-custom

Adjusted within an existing matrix.

Adjust dose, flavour or active stack within an existing matrix. Differentiate the SKU without a full custom-development cycle. Documentation route follows the same project gates.

Best for
Differentiated SKU · existing brand
Lead time
Confirmed in the quote
Start with this route 03 · Custom

Bespoke formulation and dieline.

Fully bespoke formulation, custom flavour profile and packaging dieline. The right route for category-defining launches with longer planning windows and committed quantities.

Best for
Category-defining launch · committed quantities
Lead time
Confirmed in the quote
Start with this route
Production process

Brief to released batch

Each step is reviewed before the next gate opens — across every format.

  1. 01

    Brief review

    Target market, format, quantity, claims direction.

  2. 02

    Route

    White-label, semi-custom or custom — confirmed against the brief.

  3. 03

    Spec lock

    Per-SKU specification + allergen statement drafted, then locked.

  4. 04

    Artwork

    Dieline + on-pack copy reviewed against the target-market framework.

  5. 05

    Production & QC

    In-process control plan agreed; production runs through the controlled manufacturing workflow.

  6. 06

    Batch release

    Batch-release documents are issued after production and QC release.

Documentation route

Project gates, not promises

DAT releases documentation as the project moves through each gate. Batch-release documents are issued after production and QC release.

  1. 01
    Stage
    Brief review
    Reviewed

    Target market, format, quantity, claims direction

    When

    Project entry

    Receives

    Feasibility view + working route confirmation

  2. 02
    Stage
    Formula & spec confirmation
    Reviewed

    Formulation route, allergen statement, per-SKU specification

    When

    After brief sign-off

    Receives

    Specification draft + spec-locked formula

  3. 03
    Stage
    Artwork & label review
    Reviewed

    Dieline, on-pack copy, claim wording per market framework

    When

    In parallel with spec lock

    Receives

    Reviewed artwork against the target-market framework

  4. 04
    Stage
    Production & QC
    Reviewed

    In-process control plan, stability and QC release rules

    When

    Once spec & artwork are signed off

    Receives

    Production run + in-process control records

  5. 05
    Stage
    Batch-specific documents
    Reviewed

    Per-batch QC, traceability, release-for-shipment

    When

    After production & QC release

    Receives

    Batch-specific Certificate of Analysis + traceability

  6. 06
    Stage
    Repeat order support
    Reviewed

    Forecast review, raw-material lead times, improvement notes

    When

    Per repeat order

    Receives

    Refreshed 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.

  1. 01
    Target market

    Primary distribution market and any secondary markets — drives label, claims and notification scope.

  2. 02
    Quantity

    Indicative MOQ tier and forecast for the launch window. Used to confirm route and packaging.

  3. 03
    Formula direction

    Positioning, active ingredients in scope and any non-starters. Custom development is reviewed against the brief.

  4. 04
    Packaging format

    PET bottle, doypack or sachet — pack format influences the production route and documentation set.

  5. 05
    Timeline

    Target launch window. Production calendar and raw-material lead times are confirmed in the quote.

  6. 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

EU launch guide → US launch guide → Launch checklist → Formulation guide → Launch readiness →
Manufacturing operations

DAT manages the project end to end

DAT manages gummy launches from formula selection through production, documentation review and batch release. Project-specific documentation and facility details are handled inside the project workflow where required — released to the brand owner per project stage, not as a public list.

  • Controlled manufacturing route, confirmed per project
  • Project-stage documentation; batch-specific QC release
  • Target-market review for claims, labelling and notifications
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.

Start a project Talk to our team
Quick context request

Get manufacturing context

Drop your work email and a member of the DAT team will follow up with the right context for this concept. Project documents, certificates and pricing are released through the project workspace in the DAT portal.

You will receive a short confirmation email. Project documents (specification, batch-specific COA, packaging documents) are released through the project workspace in the DAT portal once a brief is in place.