R&D
Develop a differentiated formula with prototype samples, two iterations and a manufacturing-ready handover.
Turn a product idea into a formula you can manufacture.
Our R&D team works with your brief, target market and cost targets to develop a formula that can move into production without surprises. We combine ingredient sourcing, prototype development, sensory evaluation and stability thinking from the start.
Formula development
Actives, dosages, carriers, sweeteners, flavors and appearance are balanced around your claims and your customer.
Prototype samples
We produce samples for internal review and customer testing, then refine the formula before scale-up.
Two sample iterations
Most projects include two rounds of sample adjustments to align taste, texture and performance.
What happens after R&D
Formula lock
We finalize the formula, specification and label inputs, then confirm the production path.
Pilot / scale-up
The formula is checked against production equipment, packaging and process parameters.
Quality review
Testing, batch records and COAs are prepared against the agreed specification.
Production
Approved formula moves into a scheduled production run under cGMP systems.
Formulation that respects your timeline and your margin.
Manufacturing-aware
We develop with the target dosage form and equipment in mind, reducing the gap between sample and production.
Documentation-ready
Specifications, ingredient documentation and testing support are built into the process.
Clear checkpoints
You approve the formula, sample and specification at defined stages, so there are no surprise changes at scale.
R&D questions, answered.
What is included in the R&D service?
Formula development, prototype samples, two rounds of sample iteration, specification inputs and a manufacturing handover plan. The exact scope depends on the dosage form and complexity.
How long does R&D take?
Most projects take several weeks from brief to approved sample. New actives, stability requirements or complex formats can take longer.
Can you manufacture after R&D?
Yes. R&D is designed to hand over to our production team, so the approved formula can move into sampling, scale-up and commercial production.
Is there a minimum order after R&D?
Yes. MOQ depends on the dosage form and packaging, and is confirmed with the quote before production.
Ready to build your next product?
Tell us what you want to launch. We will reply with next steps, MOQ and lead time within one business day.
- Free formula and packaging review
- MOQ from 500 units per SKU
- cGMP, ISO 22000 and HACCP production