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Bioburden testing is a fundamental microbiological analysis used to assess the level of microorganisms present on a medical device or other sterile product before it is sterilized. It involves collecting a sample from the product and then growing and counting any microorganisms present in the sample.

In vitro toxicology is the study of the potential toxicity of chemicals, pharmaceuticals, and other substances by testing them on cells or tissues. In the early stages of development, this type of study is necessary for the medical device and pharmaceutical industry, as it allows for the identification of potential hazards and side effects.

At Medistri, we’re focused on offering great services and infrastructure for healthcare companies with the task of bettering our planet. We take responsibility for our services throughout their entire cycles—from sourcing materials, managing processes to forwarding the products to our customers. We focus on the areas where we can make the biggest difference for our planet: reducing our impact on climate change, conserving important resources and using safer materials. Millions of products pass through our Sterilisation infrastructure every year. Making adjustments to reduce our carbon impact can have a meaningful impact.

Sterilization is the process of eliminating or reducing the number of microorganisms. It is a critical step in the manufacturing and packaging of medical devices and pharmaceuticals to ensure safe for use for patients. EO sterilization is a commonly used method of sterilization in the medical and pharmaceutical industries.

We are very happy to come and visit our customers to discuss their 2023 and onwards objectives!

In the medical device industry, biocompatibility evaluations are performed to assess the risk of harm to patients or users resulting from device contact with living tissue and bodily fluids. Standards such as ISO 10993 and USP Class VI provide a framework for evaluating the risk profile of a medical device, based on the nature of body contact and the duration of contact.

The LAL (Limulus Amebocyte Lysate) testing, also known as bacterial endotoxin testing, is an in vitro assay used to detect the presence and concentration of bacterial endotoxins in drugs and biological products, and is an important part of pharmaceutical microbiology.

At Medistri, you can validate your packaging according to ISTA 2A, ISTA 3A, ASTM D7386, ASTM D4169. Should you fully validate your packaging system or should you simply test one particular characteristic of your sterile barrier system, Medistri laboratory is accredited and highly experienced for the most common test method provided in ISO 11607-1.

At Medistri, we believe in delivering the highest quality services to our customers. In the sterilisation process of medical devices using ethylene oxide (EO), it is important to carefully consider several variables to ensure that the process is effective.

Medistri is attending Pharmapack 2023 in Paris, France from February 1 to 2, hosting a booth to cater client meetings, showcase its services and answer all questions.