Quality is the foundation of pharmaceutical packaging. We implement a four-stage strict quality control system for every batch of products before shipment, to guarantee stable, safe and compliant packaging materials for your drugs, vaccines and reagents.
Step 1: Supplier Audit. Before cooperation, we audit all cooperating factories, reviewing their production certifications, cleanroom environment, production records and quality management systems. Only qualified manufacturers are allowed to produce our pharma packaging items.
Step 2: First Article Check. Before mass production, we carry out first article inspection. We verify raw material quality, product dimension, appearance and material consistency. Mass production will not start until samples fully pass all testing standards.
Step3: Final Sampling Test. During and after production, every batch undergoes sampling inspection. Our QC team checks product appearance, size tolerance, sealing performance, surface coating and packaging integrity, strictly following pharmaceutical packaging industry standards.
Step4: Inspection Report. After inspection, we provide complete test data and inspection report together with shipment documents. If you require third-party independent testing, we can also arrange authorized third-party institutions to carry out testing and issue official certificates.
All our vials, rubber stoppers, aluminum plastic caps and infusion bags are produced under clean production environment, suitable for injectable drugs, lyophilized preparations, biotech reagents and veterinary medicines.
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