What is the MOQ for microneedle patch OEM?
MOQ varies with formula, custom tooling, patch size, primary pouch, carton configuration and total pack count. A standard-platform private-label program generally has a lower threshold than a new formula and custom mold. Submit your target quantity for a project-specific range.
How long do samples and mass production take?
Timing depends on novelty, tooling, feedback cycles, tests, packaging and material availability. We provide an indicative schedule after reviewing the brief and a committed schedule after specifications and commercial terms are agreed.
Can I customize the formula and needle geometry?
Yes, subject to technical feasibility and category constraints. Formula direction, active system, needle height, density, array layout, patch shape and backing can be evaluated together.
Do you provide private-label packaging?
Yes. Available scope can include barrier pouch, label, carton, insert and artwork coordination. The brand owner approves final claims, labeling and market requirements.
Are the patches compliant for the US or EU?
Compliance is product- and claim-specific. We can organize available specifications and project records, but there is no blanket global approval. The brand owner should complete qualified local regulatory, safety and label review.
Which peptides can be considered?
Potential cosmetic concepts include acetyl hexapeptide-8, copper peptides and multi-peptide systems. Compatibility, process exposure, analytical confirmation and permitted use must be reviewed for the specific formula and market.
Can I request samples before placing a production order?
Yes. A typical program uses feasibility work and samples before pilot or scale-up. Sample scope, quantity and cost are defined in the proposal.
Can you guarantee an exclusive formula?
Exclusivity depends on the development route, intellectual-property position, commercial terms and contract. It is not implied by a standard private-label order.