- Material & Sustainability Requirements
- Share destination-market requirements, preferred materials, sustainability goals and any requested blend proportion. Confirm sourcing evidence, formula compatibility, process trials, seal integrity and stability before finalizing the material specification.
- Formula Source & Iteration Goal
- Clarify whether you want to use a self-developed factory formula, modify your existing formula, transfer a proprietary recipe after NDA, or compare routes through sample iteration.
- Formula Type & Viscosity
- Specify serum, emulsion, low-viscosity fluid, or gel format. Formula type determines BFS filling-path compatibility, nozzle selection, and sealing parameters.
- Fill Volume per Vial
- Indicate target dose range (e.g. 0.5 ml to 5 ml per unit). Volume drives mold design, strip configuration, and commercial throughput planning.
- Packaging Expectation
- Define strip count per pack, snap-off or twist-open preference, secondary packaging needs, and whether custom mold development is required.
- Target Market Regulatory Scenario
- Identify primary market (CN, US FDA, EU, GCC, ASEAN). Regulatory path affects documentation, claim scope, labeling, and quality-system alignment.
- Production Stage
- Clarify whether the project is at pilot-run / stability-testing phase or ready for commercial scale-up. Stage determines checkpoint scope and timeline commitment.
- Pilot Evidence & Transfer History
- Share prior pilot data if available. Transfer behavior, seal quality results, and early stability findings help accelerate the scale-up decision gate.