New Method for Assessment of Environmental Viral Contamination of Liquids Prepared in Closed-System Drug Transfer Devices
Maya Amichay, Elana A. Slutsky Smith
Download PDFContainment performance assessment of Chemfort® (Onguard®2) closed system transfer device according to 2016 draft NIOSH protocol at first & tenth activations end of shelf life – 3PC-007
Alan-Shaun Wilkinson Ph.D; Mrs Laima Ozolina; Kate Walker Ph.D; Romana Machnikova; Professor Michael Charles Allwood Ph.D; Andrew Wallace Ph...
Download PDFChemfort® Protects Against Bacterial Contamination for 7 Days
The study confirms Chemfort®’s ability to maintain microbiological integrity even under highly challenging conditions for the 7 day test per...
Download PDFChemfort® Evaluation of Dry Connections - A Quantitative Approach
It can be concluded that no drug leakage is expected from the Chemfort® elastomer following twelve connections and disconnections.
Download PDFToxi-Guard® Protection Against Virus Penetration into Drug Vials
Both protective layers of the Toxi-Guard® air cleaning system are active against airborne viruses, and prevent the risk of virus penetration...
Download PDFChemfort® Syringe Adaptor Sterile Replacement Cap
The Chemfort® Syringe Adaptor Sterile cap is a PVC-free component and fits Chemfort® Syringe Adaptor and Chemfort® Syringe Adaptor Lock Elas...
Download PDFChemfort® Syringe Integrity
Chemfort® Syringe Adaptor Lock - Perfect alignment with commercial luer lock syringes.
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