Before your first shipment.

No. Sun Global Innovations is a sourcing and supply-chain partner. We work with qualified Chinese manufacturers and coordinate the components, private labelling, pack-out and import scope of your order. Facility photographs do not imply that we own the pictured plant.

The cartridge and branded case photographs illustrate component and packaging examples. Dimensions, materials, model, branding rights and availability need to be confirmed in your quotation. The cartridge hero is a studio-restyled version of the real supplied component photograph.

No. Private labelling and customs services do not establish product authorisation. Regulatory status depends on the exact components, finished product, intended use and destination. Relevant files must be reviewed and responsibilities agreed for your business.

Tell us the component and quantity you need for evaluation. Sample arrangements are agreed with the selected supplier. Stocked pens, cartridges and needles may be available below the indicative MOQ; availability, price and timing are confirmed with the quotation.

We review your product, specification, volume and destination, then discuss supplier options, documentation, price and lead time. Sample evaluation, artwork approvals, freight scope and importer responsibilities are agreed as applicable before the order proceeds.

We supply business customers only: licensed pharmacies, manufacturers, distributors and brand owners. There are no consumer sales or online checkout. Buyers are responsible for compliance in their own jurisdiction.

Send your company details, product or component, exact specification, intended use, destination market, volume, branding requirements and temperature requirements. We usually reply with supplier options, pricing and a lead time within two working days.

Indicative MOQs are 10,000 glass cartridges, 1,000 pen injectors, 10,000 pen needles and 5,000 nasal spray sets. API volumes are quoted on request and cold-chain shippers are arranged per shipment. MOQs vary by supplier and finish; stocked pens, cartridges and needles can ship below MOQ.

Peptide APIs are sourced from vetted GMP manufacturers with CoA per batch; supplier DMF references are available on request. Primary packaging suppliers hold ISO 15378 certification. Device and needle suppliers hold relevant ISO 13485, 510(k) and CE files. These references are supplier- and product-specific, not blanket approval for a finished kit or every market.

Yes. We coordinate cases, labels and cartons under your brand, along with case and carton design renders, label and IFU layout and GTIN/GS1 registration. Send your component and branding requirements for an OEM/ODM quotation.

We use validated PCM shipper specifications for products requiring 2–8 °C, with lane-by-lane viability checks. Typical shipper specifications cover 48–96 hours; the actual pack-out must match your product and transit lane.

Our main lanes are the US, UK, EU and GCC. Services include US bonded Importer of Record, FDA initial importer coordination and UK/EU IOR services. Availability and documentation depend on the product, intended use and destination. Other destinations can be discussed by enquiry.

No. Pricing and lead times are quoted against your specification, volume, finish, stock availability and destination. This website does not offer retail prices, instant purchases or a universal delivery promise.