Packaging & Seal Integrity

In addition to validating the design and functionality of your medical device, there are a myriad of testing requirements needed to ensure your product reaches the end user intact. From primary seal testing through to pallet-level transit testing, Eurofins Medical Device Testing network of laboratories' state-of-the-art package testing facility provides complete capabilities for evaluating every aspect of your package and labelling configurations, to ensure your product will survive the rigors of being transported around the world.

Choose Eurofins Medical Device Testing to help you:

• Validate that shipping configurations will withstand the rigours of global transit
• Assess your packaging design and material selections
• Ensure the integrity of your product’s primary sterile barrier
• Confirm your labels conform to UDI regulations and remain readable through your entire distribution channel
• Establish your product’s shelf-life through accelerated and real-time ageing

Learn about our new, state-of-the-art Package Testing Facility

Packaging integrity testing refers to various methods and processes used to assess and ensure the integrity of packaging materials, such as containers, bottles, blister packs, pouches, and other types of packaging used for medical devices and pharmaceuticals. The goal of these tests is to verify that the packaging effectively maintains its contents' quality, safety, and sterility.