How we work
OEM Manufacturing
You bring a finished formula; we manufacture it under GMP at volume, with the documentation your quality team needs. Straightforward contract manufacturing for established products.
What it is
OEM is contract manufacturing in its clearest form: you own the formula and the brand, and we turn your specification into a finished, fully documented product. Nothing about your recipe or your market positioning changes; you keep control of the specification while we take on raw-material sourcing, pharmaceutical-grade GMP production and the batch documentation your quality and procurement teams expect. Every lot is manufactured under our NSF/ANSI 455-2 certified system, tested against the specification you agreed, and released with a Certificate of Analysis your team can check line by line. Because the formula is already defined, this is the most direct route to reliable, repeatable supply, whether you are moving an established line to a new manufacturer or scaling one that has outgrown its current capacity. You own the formula and the brand; we are the accountable manufacturing partner behind every batch.
The process
How it works
From your finished specification to a dispatched, documented batch, one accountable GMP path.
Share your specification
You send your formula, target dosage form, per-batch and annual volumes, and any label or destination-market requirements, under NDA where you need one in place first. We review the formula for manufacturability and confirm scope, flagging early anything that affects sourcing, stability or the dosage form. Ownership of the specification stays with you throughout.
Quotation and sample
We quote against your exact specification, with the dosage form, batch size and packaging costed transparently. Before any full run we produce a production-representative sample, so your team can sign off on appearance, format and fit against the spec. Nothing scales up until that sample is approved.
Sourcing and qualification
We source each raw, auxiliary and packaging material to its agreed specification from qualified suppliers. Every incoming lot is checked for identity and screened for contaminants, including heavy metals and microbial limits, before it is cleared for production. Material that does not meet specification does not enter the line.
GMP production
Your batch is manufactured under our NSF/ANSI 455-2 certified GMP system, in the dosage form and at the scale your programme needs, across softgels, capsules, tablets, powders and gummies. Production runs to defined process parameters with complete batch records, so each step is documented as it happens. The same controlled process is repeated lot after lot, which is what keeps a repeat order consistent with the first.
Quality control and release
Before release, every batch is tested against its specification and formally signed off, not waved through on a loose sample. It then ships with a Certificate of Analysis, the batch records and the specification sheet your quality team files. Each lot can be traced back to the raw materials it was made from if your supplier-quality team ever needs to review it.
Packaging and dispatch
We finish and pack the batch to your agreed format, then dispatch it with the manufacturing documentation your side needs to move it into your market. Country-of-origin and other export records are prepared on request to support your import and customs process. Where responsibility passes to you as the brand owner and importer, we keep that line clear.
What this includes
Manufactured to your existing, finished specification, with no reformulation required
Available across every dosage form we run: softgels, capsules, tablets, powders, gummies and liquids
Produced under our NSF/ANSI 455-2 certified GMP system, with complete batch records
Every lot released with a Certificate of Analysis your team can check against the spec
Full raw-material qualification, with identity and contaminant testing on incoming lots
Built for consistent, repeatable, high-volume supply on a firm production schedule
Ideal for
Established brands with a finished, tested formula ready to produce at volume
Teams moving a proven product to a second or replacement manufacturer
Lines that have outgrown their current supplier’s capacity or format range
Products that need dependable, repeat supply on a firm schedule
Quality teams that need batch documentation for their supplier-qualification file
Brands consolidating several products with one GMP partner
Start a conversation
Share your product, target market and volume, our team will come back on the right route and documentation.