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Dietary supplements are made in 14 controlled stages — formulating and sourcing your ingredients, then blending, dosing, labelling, packaging, and finally testing and dispatch. As an FDA-registered, cGMP-compliant manufacturer we run every stage in-house under documented quality control, turning your brief into a finished, certified product in about 4-6 weeks.
The 14 stages · from brief to dispatch
Every stage below is a real engineering step we run in-house. Scroll through the spec sheets — the keystone card recreates an actual label pre-press dieline.
It starts on paper: your brief becomes a buildable, costed formula — every milligram accounted for before one ingredient is ordered.
We buy your formula into existence — audited suppliers, a certificate on every drum, the exact grades your label promises.
Before we make thousands, we make one perfect unit — you hold it, taste it, approve it; that golden sample locks the recipe.
Every claim, warning, and milligram is checked against the market it ships to — so your brand reads as trustworthy and stays legal.
Trust, but verify: every drum is tested and quarantined until it proves it matches the certificate — nothing unverified touches your batch.
Your formula scales up: hundreds of kilos homogenised so uniformly the last unit off the line is identical to the first.
Bulk powder becomes thousands of precise doses an hour — each weight-checked so the milligram on your label is the milligram inside.
Your label becomes an engineering drawing — every panel and millimetre fixed to the roll, the exact spec our presses print to.
The dieline goes to press: your brand colour laid down at ±0.15 mm registration, thousands of identical labels rolling off the web.
The label meets the bottle: wrapped or shrink-sleeved at 200 a minute, vision-checked so every unit wears your brand perfectly straight.
Your product gets sealed in: counted, induction-sealed, tamper-evident — the bottle a customer actually opens, protected for shelf life.
The bottle gets its box: a carton struck from its own dieline, brand-matched to the label — the unboxing your customer unwraps.
The final gate: every batch inspected, certified, and QA-signed for release — nothing ships under your brand until it has passed.
Your brand ships: palletised, climate-stored, lot-tracked, loaded — from our floor to your fulfilment, ready for your customers.
Supplements are made in 14 stages: formulation, ingredient sourcing, prototyping, regulatory label review, raw-material QC, blending, filling or encapsulation, label dieline and printing, label application, primary and secondary packaging, final QC and batch release, then warehousing and dispatch — each documented under cGMP quality control.
A private-label supplement typically takes about 4-6 weeks from approved formula to finished goods, versus a 4–6 month industry norm. Timing depends on ingredient sourcing, Certificate of Analysis testing (around 5–10 business days per lot) and your production slot.
Our minimum order quantity starts at 500 units per SKU, well below the typical 2,500–5,000-unit industry minimum. Low MOQs let you test a product in market before committing larger capital, at a slightly higher per-unit cost than full-scale runs.
Cost depends on format, active ingredients, order quantity and packaging. Capsules are the most economical to produce, while gummies and sachets cost more but command higher retail prices. We quote transparently per unit so you can model your margins before committing.
Both. You can launch quickly with a proven stock formulation or develop a fully custom formula from our ingredient library. Custom R&D adds formulation and sampling time but gives you a differentiated product you own outright.
After your formula is set we produce a small bench batch and send a golden sample to hold, taste and approve. That approved sample locks the recipe for production. Sample costs are modest and are typically credited toward your first production order.
Every incoming ingredient is identity-tested and screened for heavy metals and microbes, then quarantined until released. Production runs under cGMP with signed batch records and in-process checks, and a final Certificate of Analysis confirms the product assays at 100% of label claim.
Yes. One cGMP-manufactured product can support US FDA/DSHEA requirements, Australian TGA listing and Latin American ANVISA notification. We manufacture and document to the standard your target markets require — you own the brand and the market registrations.