The pharma-specific standard. It applies Good Manufacturing Practice to primary packaging materials — the containers and closures that touch the product — covering hygiene, contamination control, batch traceability, and validated processes.
We only source from facilities operating under internationally recognized ISO management systems — and every shipment travels with the paperwork your QA team needs to prove it.
Our partner facilities in India and China maintain certification to the standards below. Certificates are available to customers on request during supplier qualification.
The pharma-specific standard. It applies Good Manufacturing Practice to primary packaging materials — the containers and closures that touch the product — covering hygiene, contamination control, batch traceability, and validated processes.
The global baseline for quality management: documented processes, defect tracking, corrective action, and continual improvement — audited by independent certification bodies.
Certified environmental management at the factory: resource efficiency, waste and emissions control, and regulatory compliance — increasingly required by brand sustainability programs.
Worker health and safety management certified to the international standard — hazard control, incident prevention, and safe working conditions on the factory floor.
Certification scope varies by facility and product line. Current certificates for the specific facility quoted on your order are shared during supplier qualification.
Standards at the factory only matter if the documentation reaches your QA file. Ours does, on every order.
Batch-specific CoA covering dimensions, weights, and material properties against the agreed specification.
Food- and pharma-contact material declarations and resin documentation for your regulatory file.
Lot coding that traces every carton back to production date, line, and resin lot — audit-ready.
We share current ISO certificates and material declarations for the quoted facility — before you place a PO.
Qualify on real production samples, not idealized prototypes, with a CoA against your specification.
Batch documentation on every shipment, and support for your periodic supplier audits and requalification cycles.
Tell us your product line and market — we'll send the relevant ISO certificates, material declarations, and a sample plan.