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Developing innovative medical device technology is a high-risk operation.

That’s why start-up ventures to large established medical devices manufacturers use Medistri’s laboratory testing services to deliver accurate and reliable results for all their testing needs.

As Europe’s largest independent contract sterilisation company, Medistri partners with our customers through the entire process of sterilisation validation from protocol generation to final report completion.

We are very happy to come and visit our customers to discuss their 2024 and onwards objectives!

ISTA 2A standard tests a packaging system's ability to withstand the physical stress of transportation throughout the product’s supply chain to the final users.

PDMS analysis by FTIR is a test that consists of extracting and identifying PDMS residues in a qualitative/semi-quantitative method in pharmaceuticals or medical samples.

The combined resources & complete integration of expertise from our laboratory, sterilisation & quality team allow you to fully integrate the development of your products within your existing operational workflow.

The purpose is to analyse the properties of both the packaging shipping unit as well as the final product, and evaluate if the sterile barrier integrity sealing is not damaged when faced with random vibration inputs.

Three months after the launch of instagram page, we’re proud to see the growth of our community and our industry-peers on the social network.

Cytotoxicity testing is used to determine the toxicity of medical devices and materials. Cytotoxicity testing evaluates whether a material can affect living cells. Medical Device Manufacturers are required to show that their devices are not cytotoxic.

Biocompatibility is defined as “The ability of a device material to perform with an appropriate host response in a specific situation”.