VeriPac 325/LV
Micro Leak Testing Syringes, Vials and other Pharmaceutical Containers
New groundbreaking technology to verify container closure system integrity
VeriPac 325/LV is a non-destructive inspection system that offers unique integrity testing approaches, permitting highly sensitive micro leak detection of empty & pre-filled syringes, liquid filled & lyophilized vials and other rigid containers. Testing these types of products demands the highest level of sensitivity, repeatability and accuracy, and the VeriPac 325/LV is up to the task.
Applications for the VeriPac 325/LV includes the following package types:
- Empty & pre-filled syringes
- Liquid filled & lyophilized vials
- Filled & sealed bottles, cups, FFS bottles, ampoules
- Non-porous pouches
- BPC (Bulk Pharmaceutical Chemical) containers
- API (Active Pharmaceutical Ingredient) containers and bags
- BFS containers
The VeriPac 325/LV can be incorporated into protocols at any point in the handling process since it is non-destructive, non-invasive and requires no sample preparation. Applications for this technology include stability studies, clinical studies, quality assurance testing and production statistical process control (SPC). The VeriPac 325/LV is capable of detecting the slightest amount of vapor and gas release as little as 0.1 microliters. This technology is of tremendous value in the field of pharmaceutical package integrity testing to assure marketed product safety. The VeriPac 325/LV was presented and demonstrated to the FDA in March 2008 and was very well received. This test method puts the VeriPac 325/LV at the forefront of pharmaceutical laboratory equipment.
The VeriPac 325/LV core technology is based on the ASTM vacuum decay leak test method (F2338-07) recognized by the FDA as a consensus for package integrity testing. This test method was developed using VeriPac leak test instruments.