The sterility testing method in pharmaceuticals is a critical quality control procedure designed to confirm that a product is free of viable contaminating microorganisms. This test is essential for sterile pharmaceutical products, such as injectables, […]
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The Bioburden testing in pharmaceuticals is designed to assess the number and types of viable microorganisms present in a pharmaceutical product or raw materials before sterilization. This test is crucial for ensuring that the product
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Restricted Access Barrier Systems (RABS) are an advanced engineering control used in pharmaceutical manufacturing, particularly in aseptic processing. RABS are designed to provide a high level of contamination control by creating a physical barrier between
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A biological indicator (BI) is a device used to confirm the effectiveness of steam sterilization processes, specifically in autoclaves. It contains highly resistant microorganisms, usually bacterial spores, to challenge the sterilization process. If the sterilization
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Environmental monitoring (EM) is a vital part of ensuring compliance, quality, and safety in pharmaceutical manufacturing. For isolator and critical cleanrooms, maintaining controlled conditions is essential to meet stringent regulatory requirements. Isolator Technology An isolator
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RABS (Restricted Access Barrier Systems) and isolators are two advanced containment solutions widely used in pharmaceutical manufacturing to ensure sterility and minimize contamination risks. RABS provide a physical barrier, often with glove ports, allowing operators
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Learn how to prepare a SOP for settle plates of environmental monitoring by for microbial air sampling and ensuring compliance standard guideline. 1. PURPOSE To describes the procedure for monitoring airborne microbial contamination using the
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Learn how to write a SOP for Environment Monitoring Procedure in Pharmaceuticals, including acceptance criteria for temperature, humidity, and microbial counts. 1. PURPOSE To describes a procedure for monitoring the environmental conditions in pharmaceutical manufacturing
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Learn how to perform accurate moisture analysis with a detailed SOP for Karl Fischer Titration in laboratory. 1. PURPOSE To describes the steps for operating the Karl Fischer (KF) apparatus to determine the moisture content
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Learn how to write a SOP for operation of FTIR Spectrometer in pharmaceutical laboratory. 1. PURPOSE To describes the proper methods for operating the FTIR spectrometer (Fourier Transform Infrared) in laboratory. 2. SCOPE This SOP
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Learn how to write a standard SOP for operation of dissolution test apparatus in the laboratory. 1. PURPOSE To describes the process for the operation of the Dissolution Test Apparatus to ensure accurate and consistent
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Learn how to write a (Standard Operating Procedure) SOP for Good Laboratory Practices (GLP) to ensure compliance and maintain quality in laboratory environments. 1. PURPOSE To outlines the practices and guidelines to be followed to
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Learn how to write SOP for operating procedure of HPLC in pharmaceutical analysis with clear, step-by-step guidelines for efficient operation. 1. PURPOSE To outlines the procedure involved in the operation, maintenance, and troubleshooting of the
SOP for Operating Procedure of HPLC Read More »
Learn how to write a standard SOP for operation of UV-Vis Spectrophotometer in the pharmaceutical laboratory. 1. PURPOSE To describes the standard operating procedures for the operation and maintenance of the UV-Vis Spectrophotometer to ensure
SOP for Operation of UV-Vis Spectrophotometer Read More »
Learn how to write a standard procedure SOP for calibration of Karl Fischer apparatus (KF) in quality control laboratory in pharmaceuticals. 1. PURPOSE To describe the process for the calibration of Karl Fischer (KF) apparatus
SOP for Calibration of Karl Fischer Apparatus Read More »
Learn how to write a standard procedure SOP for HPLC column cleaning in quality control laboratory in pharmaceuticals. 1. PURPOSE To outline the steps for cleaning High-Performance Liquid Chromatography columns used in pharmaceutical analysis to
SOP for HPLC Column Cleaning Read More »
The Pharmaceutical Marketing System involves many strategies used to promote pharmaceutical products, including direct sales, digital marketing, and healthcare professional outreach. With a focus on global share, it examines the market distribution, competition, and trends
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Learn how to write a standard procedure SOP for calibration of UV-Vis Spectrophotometer in quality control laboratory. 1. PURPOSE To outlines the steps for the calibration of the UV-Vis Spectrophotometer to ensure accurate and precise
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Learn how to write a standard procedure SOP for calibration of FTIR apparatus (Fourier Transform Infrared) Spectrometer in quality control laboratory. 1. PURPOSE To describes the steps for the proper calibration of the Fourier Transform
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Learn how to write a standard procedure SOP for calibration of HPLC (High-Performance Liquid Chromatograph) in quality control laboratory. 1. PURPOSE To describes the procedure for the calibration of the High-Performance Liquid Chromatograph (HPLC) used
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