What Is a Nutsche Filter Isolator How is it used for HPAPI & Chemical Processing? In any pharmaceutical manufacturing operation, quality control and the safety of workers are critical factors. Working with high-potency active pharmaceutical ingredients (HPAPIs), hazardous materials, and sensitive substances often challenges traditional filtration...
How Precision Milling, Sifting, and Blending Isolators Improve Drug Safety in Pharmaceutical Production ? In drug production, being extraordinarily precise and safe is not an option. Milling, sieving, and blending are high-risk steps where product integrity and contamination control have a direct influence on the efficacy...
When it comes to containment for different pharmaceutical applications, such as API, formulation, or standalone use, Isovax is the brand to choose. We have discussed the VTD isolator that we recently made for a client in this blog. The wet mass that is transferred from the ANFD,...
Understanding Sterile: Sterility in the context of pharmaceuticals refers to the absence of all viable microorganisms, including bacteria, viruses, and fungi. Achieving sterility is paramount to prevent contamination and ensure that medical products are free from any potentially harmful agents that could compromise patient safety. Processes such...
Glove boxes, also known as isolation chambers or controlled atmosphere enclosures, are essential tools in various industries, including battery research and development. They provide a controlled environment with low levels of moisture and oxygen, allowing researchers and manufacturers to work with sensitive materials, such as...
In the realm of pharmaceuticals, precision and safety are paramount. One critical process that underscores this principle is compounding aseptic containment. To achieve impeccable sterility and minimize the risk of contamination, the compounding aseptic containment isolator stands as a cornerstone technology. In this blog post,...
Continuous development and integration of research findings and practical experiences are crucial for establishing standardized descriptions of cleanroom technology processes and specifications. The ISO standard family 14644 and VDI 2083 series of guidelines are widely used in this field. Classifying cleanrooms based on criteria, requirements,...
Fume hoods and biosafety cabinets are two examples of lab equipment that may purify the air in the work area and rid it of toxic compounds, allowing lab staff to handle hazardous materials without being concerned about contamination. They are both well known in the...
VHP decontamination systems are becoming increasingly important as regulators turn their focus away from the frequently used Steam and Dry Heat Sterilization methods in order to reduce the risk of cross-contamination and bio-burden. The VHP Passbox is used to introduce materials into the sterile area that...
Restricted Access Barrier System (RABS) is a rigid barrier consisting of transparent walls (polycarbonate or glass) and outfitted with a suitable number of glove flanges and gloves. They utilize a mix of physical and aerodynamic barriers to prevent contaminants from entering the interior environment. RABs have...