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Small Volume Parenteral (SVP) is a category of pharmaceutical preparations administered parenterally in small volumes. These sterile solutions or suspensions are packaged in vials, ampoules, or prefilled syringes. SVPs provide precise dosing and are used for intravenous, intramuscular, or subcutaneous administration. Discover their role in efficient medication delivery. svp meaning The acronym “SVP” stands for … Read more
A media fill test is a critical quality control test conducted in the pharmaceutical industry. It involves simulating the production process by filling sterile growth media instead of the actual product into containers and subjecting them to the same manufacturing conditions. This test helps assess the sterility and integrity of the manufacturing process, ensuring the … Read more
A lyophilizer, also known as a freeze dryer, is a device used to remove moisture from a substance by freeze-drying or sublimation. It is commonly used in various industries such as pharmaceuticals, food processing, and research laboratories. The lyophilization process involves freezing the substance and then applying a vacuum to remove the ice through sublimation, … Read more
(BFS) Blow fill seal technology is a highly efficient manufacturing process used for the aseptic packaging of pharmaceuticals and healthcare products. It involves blowing a plastic tube, filling it with the product, and sealing it to create hermetically sealed containers. BFS provides sterility, product protection, and extended shelf life, making it popular in the pharmaceutical … Read more
A Form Fill Seal Machine (FFS) is an automated packaging equipment that integrates the processes of forming a package, filling it with a product, and sealing it, all in a single operation. It is commonly used in various industries such as food, pharmaceuticals, and cosmetics. The FFS machine typically starts with a flat film roll … Read more
Single Use System (SUS) have gained popularity in the pharmaceutical industry due to their advantages, but they also present certain risks. This article discusses the risks of single-use systems in pharmaceutical applications, including integrity and leakage issues, material compatibility concerns, extractable and leachable, sterility assurance challenges, disposal and environmental impact, and supply chain considerations. Proper … Read more
Lyophilization, also known as freeze-drying, is a process that involves removing water or other solvents from a substance by freezing it and then subjecting it to a vacuum. This technique is commonly used in various industries, including pharmaceuticals, food processing, and biotechnology, to preserve and stabilize sensitive materials. Lyophilization helps extend product shelf life, maintain … Read more
Terminal sterilization is the process of sterilizing aseptic products, such as medical devices, pharmaceuticals, and food products after they have been packaged in a sterile environment. This method of sterilization involves exposing the products to high heat, radiation, or chemicals to kill any remaining microorganisms that may be present. Terminal sterilization is a critical step … Read more
Cleanroom validation is an essential process to ensure that cleanrooms meet the necessary standards for maintaining a controlled environment. This process involves testing and verifying the performance of the cleanroom and associated equipment, such as HVAC systems and filters. Cleanroom validation is particularly important in industries such as pharmaceuticals, biotech, and electronics, where even small … Read more
A cleanroom is a controlled environment that is designed to minimize the level of airborne particles, dust, and other contaminants that could potentially compromise the manufacturing or research processes that take place inside the room. Cleanrooms are commonly used in industries such as semiconductor manufacturing, pharmaceuticals, biotechnology, and aerospace, where even small particles or contaminants … Read more