Flair Pharma The Knowledge Kit.
Pharmaceuticals Industrial revolution
Formation of the Biofilms in purified water of pharmaceutical water systems, the threats they pose, and effective strategies for prevention and removal. Learn how to tackle biofilm-associated contamination with advanced techniques like UV light and strong disinfectants. Biofilm formation in water systems presents a significant challenge, particularly in the pharmaceutical industry. This issue not only … Read more
Discover the key differences between ULPA vs HEPA filters in terms of filtration efficiency, particle size removal, airflow, cost, and applications. Learn which filter is best suited for your needs in cleanroom and air purification environments. Two of the most advanced air filtration technologies widely used today are HEPA (High-Efficiency Particulate Air) filters and ULPA … Read more
Discover the significance of the Reynolds number in purified water systems, its role in preventing biofilm formation, ensuring water quality, and maintaining optimal flow dynamics. Learn how this crucial calculation helps regulate laminar, transitional, and turbulent flow for efficient water purification processes. Ensuring the purity of water is critical in various industrial applications, including pharmaceuticals … Read more
Incubator are essential tools in laboratories for cultivating and maintaining biological cultures in a controlled environment. The working principle of incubator allow for precise manipulation of temperature, humidity, and gas concentrations, making them indispensable across various scientific fields, including microbiology, pharmaceuticals, environmental research, and more. However, simply knowing about their role doesn’t suffice if we … Read more
Endotoxin detection and quantification are fundamental in pharmaceutical quality control, particularly due to the adverse effects endotoxins can have when introduced into the human body. Endotoxins, also known as lipopolysaccharides (LPS), are molecules that form the outer membrane of Gram-negative bacteria, and their presence in drugs can lead to pyrogenic reactions. The calculation of endotoxin … Read more
High-Performance Liquid Chromatography (HPLC) is one of the most versatile and widely used analytical techniques in chemistry and various industries, including pharmaceuticals, biotechnology, environmental science, and food safety. HPLC allows scientists to separate, identify, and quantify compounds in a sample with precision, making it an indispensable tool in research, quality control, and product development. In … Read more
High-Performance Liquid Chromatography (HPLC) has become an essential technique in analytical chemistry, used extensively for separating, identifying, and quantifying components in a sample. As demand for HPLC systems and accessories grows, numerous global suppliers offer advanced HPLC instruments, reagents, columns, and consumables. Each supplier provides unique features, technologies, and support, allowing them to cater to … Read more
High-Performance Liquid Chromatography (HPLC) plays an essential role in the pharmaceutical industry, supporting everything from drug development to quality control. Selecting the right HPLC system is critical for ensuring accurate, reliable, and efficient analyses that meet regulatory standards. The pharmaceutical sector requires precise instrumentation to handle complex workflows, varying sample types, and stringent compliance requirements. … Read more
Epoxy flooring stands out as a robust and customizable flooring option, celebrated for its unparalleled durability and adaptability. The foundation of epoxy flooring lies in the combination of two critical components: epoxy resin and a hardener. The epoxy resin serves as the binding agent, while the hardener imparts strength and stability to the mix. When … Read more
INSTALLATION QUALIFICATION IQ of RMG DETAILS OF EQUIPMENT/ SYSTEM User Department PRODUCTION Stage of Qualification INSTALLATION QUALIFCATION Equipment/System ID Equip. Location GRANULATION ROOM Equip. Make Equip. Serial No. (Supplier) TABLE OF CONTENT 1.0 PRE APPROVAL. 2.0 OBJECTIVE. 3.0 SCOPE. 4.0 EQUIPMENT / SYSTEM DESCRIPTION: 5.0 RESPONSIBILITIES. 6.0 PRE-REQUISITE. 7.0 METHODOLOGY. 8.0 DISCREPANCY … Read more