OEM / ODM FAQ
Questions B2B Buyers Ask Before Starting
Common questions about service models, formula ownership, dosage forms, MOQ and the information needed to start a project.
What is the difference between OEM and ODM supplement services?
OEM usually starts from a customer-owned formula or established product specification. ODM involves more development support around formula direction, dosage form, sensory targets or other product decisions before commercial production.
Can I bring my own supplement formula?
Yes. Existing formulas and specifications can be reviewed for dosage-form fit, ingredient availability, production feasibility, packaging requirements and destination-market needs.
Can you help develop a new supplement formula?
Yes. A project can begin with target ingredients, a benefit direction, a serving goal or a reference product, then move through feasibility review, formulation, sampling and production planning.
Which dosage forms can be developed and manufactured?
Kelrosa supports capsules, gummies, powders, softgels, tablets and liquid supplement formats. The practical route depends on the formula, serving target and commercial brief.
What determines the MOQ for an OEM or ODM project?
The practical MOQ depends on dosage form, formula complexity, raw materials, line setup, packaging components, custom printing and the selected commercial production route.
What information should I send to start a project?
Share the product idea or formula, target dosage form, serving direction, market, estimated quantity, packaging preference, timeline and any requirements that are already fixed.