Balanced DietLab

Guide · Vendor selection

How to compare supplement OEM manufacturers in Korea

Three quotes are not comparable when the assumptions differ. Here is a 12-point checklist and an MOQ table that put MOQ, cost tiers, lead time, certification and licensing support on the same axis.

  • Reply within 1–3 business days
  • MOQ from 1,000 units
  • Free consultation & quote
  • Recipe IP protection clause

At a glance — process, licensing, MOQ

Balanced DietLab standard values as of 2026-07; adjusted by dosage form, volume and export scope.

6-step OEM process
StepDurationDeliverable
1 · Concept1 weekConcept brief
2 · Formulation2–3 weeks3 formulas · COGS · claim draft
3 · Sampling2–3 weeksSamples · stability report · label
4 · Licensing & ad screening2–4 weeks (parallel)Manufacturing report · ad approval no.
5 · Mass production2–4 weeksFinished goods · lot CoA
6 · Shipping1–2 weeksDelivery · sales dashboard
Licensing & screening checklist
ItemAuthority · basisTime
Product manufacturing reportLocal authority (plant)1–2 weeks
Ad pre-screeningKorea Health Functional Food Assoc.2–4 weeks
Functional ingredient evidenceMFDS notified / individually approvedVerified at formulation
HACCP · GMPHeld by consortium plantsAlways valid
Export documents (FOB)Free-sale cert · ingredient analysis1–3 weeks
MOQ & lead time by dosage form
Dosage formMOQ (units)Standard lead time
Powder · stick1,0006 weeks
Jelly · gummy · granule2,0008 weeks
Tablet · liquid stick · pouch3,0008–10 weeks
Capsule · softgel · RTD5,00010–14 weeks

Source documents: /docs/oem-odm-process-guide.md · /docs/hff-approval-checklist.md

Common pain points

  • Quotes use different assumptions

    Grade, dosage and packaging differ, so price alone misleads.

  • Unclear licensing scope

    Confirm who handles the manufacturing report and ad screening before signing.

  • Format coverage varies

    No single plant is strong in every format.

How BDL responds

  • Same-condition quote template

    Fix formula, quantity tier and packaging so quotes become comparable.

  • Consortium line allocation

    The best-fit HACCP/GMP partner plant is assigned per format.

  • 🧪 AI formula draft + COGS

    Formula draft, cost structure and claim evidence in 3–5 minutes.

MOQ · Lead-time summary

Powder/stick 1,000 · gummy 2,000 · tablet 3,000 · capsule/RTD 5,000 · sample min 6 wks · full 8–14 wks.

FAQ for this audience

What should I compare first in a supplement OEM?

Format coverage, MOQ, unit-cost tiers, sample-to-mass lead time, HACCP/GMP certification, and licensing/ad-screening support.

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Why do quotes differ so much between plants?

Ingredient grade, dosage, excipient ratio, packaging spec, and order tier differ. Re-request quotes on an identical formula and quantity.

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OEM or ODM?

OEM if your formula and concept are set; ODM if you delegate planning. Our AI Formula Lab delivers ODM-level drafts in 3–5 minutes.

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HACCP vs GMP?

HACCP is food hazard control; GMP is the health-functional-food manufacturing and quality standard, and is mandatory in Korea.

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How do I confirm small runs are possible?

Ask for an MOQ table by format: powder/stick 1,000, gummy 2,000, tablet 3,000, capsule/RTD 5,000.

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Typical lead time?

Samples from 6 weeks; concept to shipment 8–14 weeks, with 2–4 weeks of licensing in parallel.

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Can approved (individually recognised) ingredients be used?

It depends on the supplier's rights. Confirm the usable ingredient list and recognition numbers upfront.

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What changes if I plan to export?

Destination labelling rules, ingredient regulations, English CoA/MSDS, and facility registration such as FDA.

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Which documents should I get before signing?

GMP/HACCP certificates, prior manufacturing-report cases, formula summary, stability report, and a sample lot CoA.

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What makes Balanced DietLab different?

A consortium of HACCP/GMP partner plants rather than one factory, plus AI-generated formula drafts with COGS and claim evidence.

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Related guides & FAQs

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