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Pharmaceuticals Industrial revolution
Gas chromatography (GC) is a type of chromatography technique used to separate and analyze components of a mixture based on their volatilities and affinity for a stationary phase. It involves the vaporization of a sample and its passage through a column packed with a stationary phase, where the separation occurs based on differences in partitioning … Read more
Chromatography in pharmaceuticals is a separation technique used to separate, identify, and quantify components of a mixture in order to ensure the quality, safety, and efficacy of pharmaceutical products. Chromatography involves the separation of a sample into its individual components based on their physicochemical properties using a stationary phase and a mobile phase. The stationary … Read more
21 CFR Part 11, also known as Title 21 Code of Federal Regulations Part 11, is a regulation issued by the U.S. Food and Drug Administration (FDA) that sets forth the requirements for electronic records and electronic signatures in the pharmaceutical, biotechnology, and medical device industries. It applies to pharmaceutical companies, contract research organizations (CROs), … Read more
View Post HPLC (High-performance liquid chromatography) is used to separate, recognize, and measure components in mixtures. It is a type of chromatography that uses a liquid mobile phase to move a sample mixture through a column packed with a stationary phase. Hplc is a very important and common instrument of the Quality Control Lab. In … Read more
Technology transfer in the pharmaceutical industry is a critical step in bringing a new drug or medical device from the laboratory to the market. It involves transferring knowledge, expertise, and technology from the research and development phase to manufacturing, quality control, and regulatory compliance. Technology transfer is essential to the process of discovering novel drugs … Read more
Environmental Monitoring In Pharma Industry means the process of regularly testing and analyzing the air, water, surfaces, and equipment of the manufacturing plant of the pharmaceutical facility. This is to ensure that the environment is free from contamination that could potentially compromise the quality, safety, and efficacy of the drugs being produced. This area’s monitoring … Read more
There are Different sources of Contamination in Aseptic Area. An aseptic area is a premise in a clean area, designed, constructed, serviced, and used with the intention of preventing microbial contamination of the product. It is essential to identify the sources from which the contaminants can enter the aseptic area in order to avoid the … Read more
Various batch coding machines are needed by different businesses in order to print codes and data on a variety of products and packaging. In this article, we’ll walk you through the specifics of two different technologies to help you understand how industrial batch coding machines function and where they’re used. Equipment that performs batch coding … Read more
Dry heat sterilization is a very commonly used process in sterile pharma plants. The most affordable and well-liked sterilizing method for medical supplies and equipment is dry heat sterilization. Microorganisms are destroyed during steam sterilization when they are exposed to pressurized steam. Dry heat sterilization uses temperatures as high as 370ºC to inactivate bacteria, which … Read more
Tray dryer in pharma industries is an enclosed, insulated chambers, trays are piled on top of one another in tray dryers, which use conventional drying. The driers are used in industrial manufacturing processes where drying and heating are essential steps, including the production of food goods, pharmaceuticals, dyes, and chemicals, among others. The trays are … Read more