Custom Gummy Formulation
Bespoke gummy development for brand owners whose dose, claim intent, or sensory profile cannot be served by a pre-validated base.
What DAT Supply Provides
DAT Supply runs custom-formulation projects from initial brief through stability data delivery. Each project is scoped against the requested target market: dose ranges, claim wording, and label format are reviewed before production scheduling. The deliverable is a locked specification, a pilot batch, and a documentation handover.
How We Work
The brief is translated into a development plan with target dose, sensory profile, and packaging format. Bench prototypes are produced and reviewed with the brand owner before pilot scaling. The pilot batch is placed on stability and the specification is locked once intermediate data confirms the position.
Documentation Delivered
The handover pack covers the locked specification, ingredient declaration, allergen statement, and stability position at the agreed timepoints. Additional documents are added on request when the importer of record or retail customer requires them. Documentation is reviewed against applicable target-market frameworks.
Frequently asked questions
How long does custom formulation take
Typical projects run several development cycles before lock. The exact duration depends on dose complexity, sensory targets, and stability requirements; a stage plan is issued at project start.
Who owns the resulting formulation
Ownership is set in the project agreement. Brand owners typically commission either an exclusive formulation or a variant of a DAT Supply base.
Do you support claim substantiation work
DAT Supply scopes claim wording against applicable target-market frameworks and flags claims that require external substantiation before label use.
Related
Start a feasibility brief
Send the brief through the DAT portal. Our team responds the same working day with format-fit notes and a project roadmap.