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Quality & ISO standards

Certified at the source. Documented to your dock.

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.

The standards

Four ISO systems behind every order.

Our partner facilities in India and China maintain certification to the standards below. Certificates are available to customers on request during supplier qualification.

ISO 15378
GMP · Primary packaging for medicinal products

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.

What it means for youContainers manufactured under pharma-grade GMP discipline, with traceability from resin lot to finished container.
ISO 9001:2015
Quality management systems

The global baseline for quality management: documented processes, defect tracking, corrective action, and continual improvement — audited by independent certification bodies.

What it means for youConsistent dimensions, gram weights, and neck tolerances batch after batch, with a formal CAPA process if anything drifts.
ISO 14001:2015
Environmental management systems

Certified environmental management at the factory: resource efficiency, waste and emissions control, and regulatory compliance — increasingly required by brand sustainability programs.

What it means for youA supply chain you can defend in your own ESG reporting, with environmental data available for supplier scorecards.
ISO 45001:2018
Occupational health & safety

Worker health and safety management certified to the international standard — hazard control, incident prevention, and safe working conditions on the factory floor.

What it means for youEthical-sourcing confidence: the people making your packaging work in independently audited safe conditions.

Certification scope varies by facility and product line. Current certificates for the specific facility quoted on your order are shared during supplier qualification.

With every shipment

The paperwork arrives with the pallets.

Standards at the factory only matter if the documentation reaches your QA file. Ours does, on every order.

Doc 01

Certificate of Analysis

Batch-specific CoA covering dimensions, weights, and material properties against the agreed specification.

Doc 02

Material compliance

Food- and pharma-contact material declarations and resin documentation for your regulatory file.

Doc 03

Batch traceability

Lot coding that traces every carton back to production date, line, and resin lot — audit-ready.

Supplier qualification

Qualify us the way you'd qualify any supplier.

Step 01

Certificates & declarations

We share current ISO certificates and material declarations for the quoted facility — before you place a PO.

Step 02

Samples from production tooling

Qualify on real production samples, not idealized prototypes, with a CoA against your specification.

Step 03

Ongoing surveillance

Batch documentation on every shipment, and support for your periodic supplier audits and requalification cycles.

Start qualification

Request the certificate pack.

Tell us your product line and market — we'll send the relevant ISO certificates, material declarations, and a sample plan.