Sun Global Innovations / Sourcing & quality
Qualified sources. A coordinated supply chain.
We source from qualified Chinese manufacturers rather than presenting every component as our own production. Our Shenzhen operations coordinate sourcing, factory audits, quality control and pack-out.
01
Peptide API sourcing
Bulk actives are quoted against your specification and volume. We source from vetted GMP manufacturers, with a certificate of analysis per batch and supplier DMF references on request.
GMP / CoA per batch
02
Primary packaging
Glass cartridges, vials, stoppers and nasal spray components are sourced against the required material, dimensions and supplier quality documentation.
ISO 15378 supplier plants
03
Device suppliers
Reusable and disposable mechanical pens and sterile pen needles are sourced from manufacturers holding the relevant quality and regulatory files.
ISO 13485 / Relevant 510(k) and CE files
04
Private-label build
Your brand is carried through the case, labels and cartons. We coordinate design renders, IFU layout and GTIN/GS1 registration as part of the requested build.
OEM / ODM
05
Cold-chain pack-out
Validated PCM shipper specifications are matched to the transit lane. Product requirements, shipment size and journey duration inform the pack-out.
2–8 °C / Lane-by-lane checks
06
Import coordination
The order and its documentation are coordinated for the destination market, including US Importer of Record, customs bond and FDA initial importer coordination.
US / UK / EU / GCC
From your supplied photographs
A closer view of the source.
Facility visits bring the conversation closer to manufacturing. The photographs below show a facility exterior, production-area visits and technical discussions. Product-specific qualification is assessed through the relevant documentation, not inferred from a photograph.
Images illustrate visits and components, not ownership of the facility, a named partnership or certification of a particular product.
What gets reviewed before an order.
A useful quality review connects the supplier’s documents to the exact item you intend to buy. The scope is agreed against your product and destination, not inferred from a facility photograph.
Supplier identity & scope
Confirm the manufacturing source and whether its quality certificate covers the relevant activity and component.
Specification & samples
Agree the component drawing, material and acceptance criteria, along with any sample evaluation required before volume supply.
Product & batch records
Review the relevant regulatory files and batch documentation. API enquiries include CoA per batch; other records depend on the product.
Changes & handover
Clarify artwork approvals, component revisions, packing conditions and receiving requirements in the order scope.
Certificates and regulatory files are product- and supplier-specific. Share your intended use and target market so the required documentation can be reviewed for your quotation.
Tell us what you need to ship.
Product, destination market and volume. One point of contact.