Tag: Storage Conditions for Drugs

SOP for Implementing Stability Testing for Export Products According to ICH Q1F Standard Operating Procedure for Stability Testing of Export Products Following ICH Q1F 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability testing for drug products intended for export to markets covered by ICH Q1F guidelines to…

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SOP for Interpreting ICH Q1B Photostability Testing Guidelines Standard Operating Procedure for Conducting Photostability Testing Following ICH Q1B 1) Purpose The purpose of this SOP is to provide guidance on conducting and interpreting photostability testing in accordance with ICH Q1B guidelines to ensure that drug substances and products are not adversely affected by exposure to…

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SOP for Conducting Stability Testing in Accordance with WHO Guidelines Standard Operating Procedure for Stability Testing Following WHO Guidelines 1) Purpose The purpose of this SOP is to establish a procedure for conducting stability testing in compliance with the World Health Organization (WHO) guidelines to ensure the safety, efficacy, and quality of pharmaceutical products. 2)…

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SOP for Preparing Stability Data for US FDA Submissions Standard Operating Procedure for Compiling Stability Data for FDA Submissions 1) Purpose The purpose of this SOP is to provide a standardized procedure for preparing and compiling stability data in a format suitable for submission to the US FDA to support New Drug Applications (NDAs) and…

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SOP for Designing Stability Studies in Compliance with ICH Q1A(R2) Guidelines Standard Operating Procedure for Designing Stability Studies Following ICH Q1A(R2) Guidelines 1) Purpose The purpose of this SOP is to establish a standardized approach for designing stability studies in compliance with the ICH Q1A(R2) guidelines to ensure that drug substances and products maintain their…

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SOP for Assessing Stability of Drug Products Under Extreme Environmental Conditions Procedures for Stability Testing of Drug Products in Harsh Conditions 1) Purpose The purpose of this SOP is to outline a standard procedure for conducting stability studies on drug products exposed to extreme environmental conditions, such as high temperatures, freezing, and varying humidity levels….

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SOP for Assessing Stability for Drug Products in Extreme Conditions Guidelines for Stability Testing of Drug Products Under Extreme Conditions 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on drug products under extreme conditions. Stability testing ensures that drug products maintain their safety, efficacy, and quality…

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SOP for Conducting Stability Studies for Temperature-Sensitive Biologics Guidelines for Stability Testing of Temperature-Sensitive Biologics 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on temperature-sensitive biologics. Stability testing is necessary to ensure that these biologics maintain their safety, efficacy, and quality under various storage conditions throughout…

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SOP for Performing Stability Studies for Sterile Products Guidelines for Stability Testing of Sterile Products 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on sterile products. Stability testing is essential to ensure that sterile products maintain their sterility, safety, efficacy, and quality under various storage conditions…

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SOP for Assessing Stability for Enzyme-Based Drugs Guidelines for Stability Testing of Enzyme-Based Drugs 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on enzyme-based drugs. Stability testing is essential to ensure that enzyme-based drugs maintain their activity, safety, efficacy, and quality throughout their shelf life under…

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