Quality & documentation
Verified at source. Documented to destination.
Sterlington sources exclusively from GMP-certified manufacturers and accompanies every order with the documentation your regulator and your inspectors expect to see.
Sourcing standard
GMP-certified manufacturers only. No exceptions.
Every product in the SterliX range is sourced from a facility holding current Good Manufacturing Practice certification. This rule does not bend for cost, urgency or availability pressure.
Before a product is listed, the manufacturer completes supplier due diligence. Before a product ships, its documentation is checked against the order. This is the whole basis of the relationship we ask partners to trust.
Zero compromise on sourcing
Only GMP-certified manufacturers, qualified before listing.
Documentation on every order
Certificates of Analysis, GMP certificates and batch records, inspection-ready.
Traceable end to end
Tracked, temperature-controlled logistics with full batch traceability.
The process
Six controlled steps.
- 01
Supplier qualification
We verify the manufacturer's GMP certification and complete due diligence on the facility and the product before anything is listed. A product without a qualified source is not offered.
- 02
Product verification
For each order we check the product specification, the Certificate of Analysis for the batch and the remaining shelf life against what you have asked for, before release.
- 03
Documentation package
We compile the Certificate of Analysis, the manufacturer's GMP certificate, batch records and the import documentation you need for your local regulatory submission.
- 04
Cold-chain logistics
Transport is temperature-controlled from the manufacturer to your warehouse and tracked throughout, so product condition is protected on the route.
- 05
Traceability
Every unit can be followed by batch from the manufacturer to the destination, supporting recalls, audits and inspections.
- 06
Post-delivery follow-up
We confirm receipt and condition after delivery and remain available for documentation and regulatory queries.
Documentation
What accompanies every order.
Documentation is prepared for the batch you receive, not as a generic pack, so it can be submitted and inspected as it stands.
Request product documentationCertificate of Analysis
Batch-specific analytical results issued by the manufacturer.
GMP certificate
The manufacturer's current Good Manufacturing Practice certification.
Batch records
Batch identification and release documentation for traceability.
Import documentation
Shipping and import certificates prepared for your market.
Scope of supply
What we do, and what we do not do.
We do
- Supply licensed distributors, hospitals and institutional buyers
- Source from GMP-certified manufacturers only
- Provide batch documentation with every order
- Verify partner licences before the first shipment
We do not
- Sell or ship medicines to the public
- Supply without the appropriate licences and registrations
- Publish dosing or clinical guidance on this website
- Substitute products without written agreement