Learn how to write SOP for Handling Deviations. Ensure compliance, document deviations effectively, and implement corrective actions to maintain quality standard. 1. PURPOSE To describes a standard procedure for identifying, documenting, investigating, and resolving deviations […]
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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
SOP for Good Laboratory Practices (GLP) Read More »
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
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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
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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
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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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Learn how to write a standard procedure SOP for calibration of dissolution test apparatus in quality control laboratory in pharmaceuticals. 1. PURPOSE To describe of this Standard Operating Procedure (SOP) is to provide a standardized
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Learn how to write a standard procedure for Product Development Planning in pharmaceutical industry. 1. PURPOSE To outlines the steps and guidelines for planning product development, ensuring that all necessary tasks are completed in a
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Learn how to write the Standard Operating Procedure (SOP) for basic GMP requirements in production area, ensuring quality and compliance in pharmaceutical manufacturing environments. 1. PURPOSE To describe a basic rules for Good Manufacturing Practices
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Learn how to write a standard SOP for disposal of rejected materials (raw and finished products) in the pharmaceutical industry. 1. PURPOSE The purpose of this procedure is to establish a system for the destruction
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Learn how to write a standard procedure for handling & usage of hazardous chemicals in quality control laboratory. 1. PURPOSE The purpose of this SOP is to describe the procedure handling & usage of hazardous
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Learn how to write standard procedure for sampling method of packaging materials in the pharmaceutical industry. 1. PURPOSE The purpose of this procedure is to describe sampling method of packaging materials for ensuring the identity
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