Your end-to-end OEM workflow
- 01
Gather requirements
Target market, formula direction, caffeine target, pouch format and quantity.
- 02
Targeted R&D
Review ingredient documents, compatibility and development feasibility.
- 03
Sample testing
Compare sensory attributes and agree the analytical requirements.
- 04
Finalize sample
Record the approved formulation and reference sample.
- 05
Tailored design
Develop the can label, pack information and carton artwork.
- 06
Approve design
Check artwork, ingredients, warnings, codes and dimensions.
- 07
Sign contract
Confirm specification, quantities, responsibilities and commercial terms.
- 08
Box prototyping
Check can, label and carton prototypes as an assembled pack.
- 09
Approve prototype
Approve the final packaging and controlled production reference.
- 10
Start production
Proceed against the approved specification and agreed release plan.
Approval protects the brief
The sample, formula, artwork and packaging prototype become controlled references. Changes to caffeine source, flavor, ingredient form or can construction need a recorded review, even when the product name stays the same.
A clearer brief. A better starting point.
Tell us your caffeine target, flavor, can format and destination market. Production starts at 3,000 cans per SKU and 9,000 cans per order.