A defined six-stage process from requirement review to delivery. You know what happens at each step, what it costs and what documentation comes with it — before you commit.
Comprehensive private label flexibility covering dieline packaging, formula specifications, and regulatory multi-language localization.
Regulated manufacturing safeguards protecting distributor qualification and cross-border customs clearance.
Strict production controls under audited ISO 13485 scope.
Only authentic CoA parameters and verified technical dossiers.
Direct supply to verified medical distributors and clinic groups.
MOQ & Lead Times
Transparent minimum order quantities and realistic lead times for neutral stock, private label, and full custom formulations.
The process
Each stage produces something concrete. Nothing moves forward until the previous stage is settled.
You tell us the product category, target market, packaging direction and indicative volume. We confirm what is feasible at that scale before any commitment.
We map your brief against the available formulations — HA dermal fillers, skin boosters, PN/PDRN, PLLA, CaHA, exosome or meso solutions — and shortlist what fits.
Logo, retail box, label, leaflet and blister paper are prepared against your artwork. Local labeling requirements are confirmed with your importer or agent.
Samples are dispatched for evaluation alongside the technical specification sheet and the documentation that is available for your market.
Production runs under the manufacturing quality management system. Quality control records and batch documentation follow the production lot.
Shipping documentation is prepared, including air transport classification documentation for hyaluronic acid gel where applicable.
Packaging
Retailing an injectable product means the packaging has to satisfy two audiences at once: your brand identity and your market’s labeling requirements. We work on both together.
Documentation
Documentation is the part of OEM most often left vague. Here is what is actually available and what remains your importer’s responsibility.
Product registration and market authorization are separate from quality management system certification and follow each market’s local pathway.
View quality & certificationsDistributor support
Most distributor inquiries are portfolio-level rather than single-SKU. We can help you map a coherent range against your channel and market, then support it with documentation.
Category-level selection across fillers, boosters, regenerative and biostimulator lines so the range holds together.
Physical samples dispatched by express courier for professional evaluation before a volume commitment.
Specification sheets and available quality documentation supplied for your supplier qualification file.
Packaging and label copy adapted for your market, with local requirements confirmed through your importer or agent.
Buyer questions
MOQ depends on the specific formulation, packaging configuration and artwork complexity. Because these vary per project, we confirm the applicable MOQ at the requirement review stage rather than publishing a single blanket figure.
Logo, retail box, label, leaflet and blister paper can all be customized, along with scale stickers and additional printed materials where applicable.
Lead time depends on whether stock product or a custom configuration is required, and on the artwork approval cycle. A concrete schedule is provided with the quotation.
We provide technical specification sheets and the quality management documentation that has been issued. Registration itself follows each market’s local pathway and is normally handled by your importer or appointed agent.
Yes. Distributor support includes portfolio selection across categories, so you can build a coherent range rather than sourcing individual products independently.
Request for quotation
Direct response with technical specifications, tiered quotation and country-specific documentation status.
