Each phase of our production process is conducted in cGMP compliant facility equipped with the latest generation equipment within certified clean rooms [ ISO 8 (class 100,000), ISO 7 (class 10,000), ISO 5 (class 100)] using validated processes.
Vials are washed with lab grade distilled water and then by Isopropyl Alcohol (IPA) before Dry Heat Sterilization.
After Dry Heat Sterilization, each vial is sealed with steam sterilized (autoclaved) rubber stopper and steam sterilized (autoclaved) aluminum seal and then further packed in tamper proof Ethylene Oxide (ETO) sterile plastic bags to maintain sterility during storage and transit.
These tubular USP/EP TYPE I injection vials are formed as per international DIN/ISO 8362-1 standards and are available in 2R, 4R, 6R, 10R, 15R, 20R and 30R sizes. Amber glass vials also available for bulk orders.
Sterility Test Report from NABL Accredited Lab available at extra cost.
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Each phase of our production process is conducted in cGMP compliant facility equipped with the latest generation equipment within certified clean rooms [ ISO 8 (class 100,000), ISO 7 (class 10,000), ISO 5 (class 100)] using validated processes.
Vials are washed with lab grade distilled water and then by Isopropyl Alcohol (IPA) before Dry Heat Sterilization.
After Dry Heat Sterilization, each vial is sealed with steam sterilized (autoclaved) rubber stopper and steam sterilized (autoclaved) aluminum seal and then further packed in tamper proof Ethylene Oxide (ETO) sterile plastic bags to maintain sterility during storage and transit.
These tubular USP/EP TYPE I injection vials are formed as per international DIN/ISO 8362-1 standards and are available in 2R, 4R, 6R, 10R, 15R, 20R and 30R sizes. Amber glass vials also available for bulk orders.
Sterility Test Report from NABL Accredited Lab available at extra cost.
Buy from Amazon