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Sterilisation

Mixed Load Sterilisation Validation

Mixed Load Sterilisation Validation is crucial for ensuring the efficacy and safety of medical devices. It verifies that sterilisation processes effectively treat diverse loads containing various materials and configurations, meeting stringent regulatory standards. Medistri excels in providing robust validation services, ensuring compliance and reliability in sterilisation practices.

Laboratory

Bisphenol Testing

Bisphenols are compounds used in the industrial manufacture of plastics, as monomers of polycarbonate or as additives in epoxy resins. They form a large family made up of many substances that have similar chemical structures and uses.

Sterilisation

Mixed Load Cycles

Ensuring the safety and effectiveness of medical instruments is crucial in healthcare. One advanced method for achieving this is through Mixed Load Cycles, where different types of instruments are sterilized together in a single cycle. This approach not only saves time but also improves operational efficiency in medical settings.

Laboratory

Phthalate Analysis Testing

Phthalates are a series of widely used chemicals that demonstrate to be endocrine disruptors and are detrimental to human health. Phthalates can be found in most products that have contact with plastics during producing, packaging, or delivering.

Laboratory

Haemocompatibility

Haemocompatibility, also known as hemocompatibility, is a crucial aspect of biocompatibility testing for medical devices that come into contact with blood. It evaluates the interactions between the medical device and blood components to ensure that the device does not adversely affect blood or cause harmful reactions when used as intended.

SVC announces Medistri as Top 5 PME in Suisse Romande

Medistri, a leading provider of sterilization and logistics solutions for the medical and pharmaceutical industries, is proud to announce that it has been recognized as one of the top five small and medium-sized enterprises (SMEs) in Suisse Romande by the prestigious Swiss Venture Club (SVC). This nomination is a testament to Medistri’s commitment to innovation, quality, and excellence in service.

Laboratory

GC/MS Compliance

GC/MS Analysis (also called Gas Chromatography/ Mass Spectrometry) is an analytical process that utilises the capabilities of Mass Spectrometry and Gas Chromatography in order to determine the chemical compounds within a sample.

Laboratory

Bacterial Endotoxins Validation

Bacterial Endotoxins Validation is a critical process in the pharmaceutical industry that ensures the safety and quality of products. Endotoxins from gram-negative bacteria are the most common cause of toxic reactions resulting from contamination of pharmaceutical products.

Packaging

Rotational Drop Test

Rotational Drop Test is crucial as it evaluates a package’s ability to withstand shocks during shipping. It aids in improving package design, reducing costs associated with damaged goods, ensuring compliance with industry standards, and preventing over-packaging and under-packaging. It’s a key part of ensuring product safety and integrity during transportation.

Laboratory

GC/MS Residual Analysis

GC/MS Residual Analysis is crucial primarily for safety reasons. Residual solvents can be harmful or toxic. Even if they are not directly harmful, they can react with other substances in the product to form harmful compounds. Therefore, it’s essential to identify and quantify them to ensure the safety of the product.