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Manufacturing / Softgels

Softgels — the format for oil-active stacks and lipid-soluble vitamins.

Gelatin or plant-based shell options, project-managed inside the quality-controlled supply chain.

Shell
Gelatin · Plant-based
Routes
Semi-custom · Custom
Pathways
EU · UK · US
Softgels — the format for oil-active stacks and lipid-soluble vitamins. — DAT Supply manufacturing
Working routes
3

white-label · semi-custom · custom.

Project gates
4

brief · spec · artwork · release.

Pathways
EU · UK · US

reviewed per target-market framework.

Format manifest

Softgels are the format of choice for oil-actives — omega-3, vitamin D, CoQ10, MCT-based stacks. The fill chemistry is reviewed before spec lock so what ships matches what was promised.

Softgels at a glance
Shell
Gelatin · Plant-based
Fill
Oil-active
Best routes
Semi-custom · Custom
Gates
Brief · Spec · Artwork · Release
Best-fit use cases

When softgels fit

Softgels are right when the active is lipid-soluble or oil-based, when the brand needs a premium clinical SKU, or when the active dose would oxidise in a non-protected format.

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.

Packaging options

PET bottle · Blister

Softgel packaging is confirmed per project — PET bottle is canonical; blister suits pharmacy-channel SKUs.

  1. PET bottle

    Canonical supplement-shelf format for 30/60/90-day daily-use ranges.

  2. Blister

    Pharmacy-channel premium presentation.

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.

Related product concepts

Concepts reviewed for this format

A short pick of reviewed concepts. Final positioning, claims and documentation are reviewed per project.

Explore the full product catalogue →

Related ingredients

Common actives for this format

Frequently asked questions

  • Are plant-based softgel shells available?

    Yes — plant-based shells are routine alongside gelatin. Shell choice is confirmed during the brief against the active list.

  • Why a softgel rather than a capsule?

    Softgels protect oil-active and lipid-soluble actives that would not perform inside a hard-shell capsule. Active selection drives the format choice.

  • Is white-label available for softgels?

    Softgels typically route through semi-custom or custom because the fill chemistry is part of the spec. White-label availability is confirmed per project.

  • What documentation gates apply?

    Brief review, spec confirmation, artwork review per the target-market framework, and batch-specific Certificate of Analysis after QC release.

  • What is the order of magnitude for a first run?

    Semi-custom starts from 2,500 units; custom development from 5,000 units. Final volumes are confirmed in the quote.

Project handoff

Request a softgel quote

Send the brief — DAT will confirm shell choice, review fill chemistry and frame the spec lock.

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.