Preventing leaks and seal failures in sterile packaging is vital for patient safety. Learn how vacuum decay and airborne ...

PTI Inspection System’s VeriPac 310 leak detection and package integrity testing system reduces waste and provides the user with a clear evaluation of package integrity. PTI Inspection System’s ...

Revisions to USP General Chapter may impact evaluation of sterile product package integrity. A proposed revision of the United States Pharmacopeia (USP) General Chapter <1207>, Sterile Product Package ...

PTI introduces the next generation VeriPac Inspection System, the VeriPac 310. This new model replaces the popular first generation VeriPac 225 and 325 test systems. The new VeriPac 310 is ideal for ...

False positives can occur when performing sterile integrity testing. Understanding how to identify them can help minimize their occurrence in future package designs. By Curtis L. Larsen Some medical ...

At different stages of the drug lifecycle, the minimum provision for parenteral products is a safety barrier against potential contaminants. This protection is guaranteed by selected container closure ...

A medical device's package plays a key role in safely delivering treatment to patients. It must ensure the integrity of the device from the point of manufacture to the point of final use. In addition, ...

Deterministic, non-destructive seal integrity testing delivers validated, quantitative results. Learn why this method ...