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Medistri is attending Pharmapack 2025 in Paris, France from January 22 to 23, hosting a booth to cater client meetings, showcase its services and answer all questions.

EO Sterilisation is particularly beneficial for products that cannot be subjected to high heat or moisture, making it an ideal solution for many modern medical devices and pharmaceutical products. Here’s how it works in practice for different types of products that are in their definitive package.

The MDR (Medical Device Regulation) certification for sterile kits refers to the regulatory requirements that apply to the manufacturing, distribution, and use of medical devices, including sterile kits, within the European Union. Sterile kits often consist of a combination of medical devices, instruments, or other items assembled into a single product for medical procedures. It sets forth requirements for the design, manufacture, and distribution of medical devices to ensure their safety and effectiveness.

A pharmaceutical vial is a small container, typically made of glass or plastic, used to store and protect liquid, powder, or lyophilized (freeze-dried) pharmaceutical substances. These vials must be sterilized and sealed with a rubber stopper or a screw-on cap, often secured by a metal crimp or seal. They are commonly used for injectable medications, vaccines, or other substances requiring precise dosing. Vials ensure the contents are protected from contamination and maintain sterility until use.

Ethylene oxide (also known as EO or EtO) is a low temperature gaseous process widely used to sterilize a variety of healthcare products, such as single-use medical devices. Through the use of a vacuum-based process, EO can efficiently penetrate surfaces of most medical devices and its lower temperature makes it an ideal process for a wide variety of materials.

MTT Assay is a colorimetric assay that measures the metabolic activity of cells as an indicator of their viability. By leveraging the cell's natural enzymatic processes, this assay transforms a yellow tetrazolium salt (MTT) into insoluble purple formazan crystals. These crystals only form in cells with active metabolism, offering a direct correlation between formazan production and the number of living cells.

The Swiss Venture Club is renowned for its dedication to promoting and supporting entrepreneurship, innovation and highlighting successful companies for over 20 years throughout the eight economic regions in Switzerland.

Subacute Systemic Toxicity is a critical aspect of health risk assessment that evaluates the effects of exposure to harmful substances over a period longer than immediate (acute) but shorter than chronic. This type of toxicity is essential in occupational safety, environmental health, and the development of medical and pharmaceutical products, as it helps to identify potential health risks that emerge from prolonged exposure.

Gas Chromatography-Mass Spectrometry (GC/MS) is a powerful analytical technique widely used to identify and quantify impurities in various fields such as pharmaceuticals, environmental studies, and food safety. By combining gas chromatography (GC) and mass spectrometry (MS), GC/MS provides detailed and reliable data crucial for ensuring product purity and safety.

Routine LAL (Limulus Amebocyte Lysate) testing and bacterial endotoxin determination are crucial for maintaining product safety and quality. By consistently performing these tests, companies ensure that their products meet regulatory standards, protect patient health, and uphold their reputation.