From enquiry
to delivery.
Nine stages from first contact to repeat order — each with a documented hand-off, so you always know where your project stands.
The nine stages
A documented path.
Nothing advances without the previous stage closing out — the same discipline an auditor expects.
Enquiry & NDA
We scope your product, volume and timeline, and put an NDA in place.
Feasibility & quotation
We confirm we can make it to spec and issue costed options.
Formulation & sampling
Bench development and samples against your brief, iterated until signed off.
Pilot batch
A small-scale batch validates the process before committing to production.
Registration & regulatory
Full dossier and technical support for NPRA / KKM and export markets — handled end to end.
Scale-up
Process transferred to full production scale with parameters locked.
Production
Manufactured under GMP against the master batch record.
QC release
In-house testing and independent QA sign-off before anything ships.
Delivery & reorder
Finished goods dispatched, with retained samples and records on file for reorder.
Timeline
How long it takes.
Lead times depend on format, registration and volume. Indicative ranges are confirmed at quotation.
New formulation
Brief to approved sample — varies by formulation.
Pilot to scale-up
Validated pilot to first production — varies by volume.
Repeat order
Reorder of an established product — from about 1 week.
Let's talk production.
For manufacturers, distributors and brand owners who need GMP- and ISO 22000-grade production at scale.