Discover your next big idea for life sciences at PACK EXPO Las Vegas
Experience a breakthrough in life sciences packaging—explore solutions from 2,300 suppliers spanning all industries, all in one place this September

Sepha: Leak testing and inspection system

Sepha’s Multi-Q is a multi-functional, non-destructive leak testing and inspection system for rigid containers and flexible packaging.

Multi-Q
Multi-Q

System offers an all-in-one solution to test the integrity of all types of containers including sachets, pouches, bags, bottles, vials, ampoules, trays, devices, and modified atmosphere packaging (MAP).

Using non-destructive methods including vacuum decay (ASTM F 2338-09 (2013)), pressure decay ramp to proof pressure, occlusion, and a vacuum flexible membrane, the Multi-Q provides the flexibility to test different containers in variable sizes for defect types including cracks, channels, gross holes as well as pinholes down to 5μm.

The lab-scale unit has a small footprint and offers the flexibility to switch between test attachments depending on product and specified test requirements. Test attachments can be easily changed and can be automatically detected by the system once in place. The relevant recipes for the selected attachment will be available to start testing immediately.

The non-destructive and deterministic test methods provide quick, reliable and repeatable results enabling customers to improve the accuracy of their leak detection procedures and reduce cost as the method prevents the packaging from being damaged.

Break out of the ordinary: see what’s new in life sciences packaging
<strong>At PACK EXPO Las Vegas, you’ll see machinery in action and new tech from 2,300 suppliers, collaborate with experts and explore transformative solutions. Join us in September to experience a breakthrough for life sciences products.</strong>
REGISTER NOW & SAVE!
Break out of the ordinary: see what’s new in life sciences packaging
FDA warning letters surge - is your team prepared?
New guide reveals expert strategies to prevent regulatory issues and respond effectively to FDA enforcement actions in pharmaceutical and medical device manufacturing.
Read More
FDA warning letters surge - is your team prepared?