Pharma Stability: Insights, Guidelines, and Expertise
How to Implement Stability Studies for Drug Products in Compliance with US FDA CFR Title 21 Conducting Stability Studies for Drug Products as per US FDA CFR Title 21 Requirements Introduction Stability studies are essential for ensuring that drug products meet their quality, safety, and efficacy standards throughout their shelf life. The US Food and…
SOP for Performing Stability Studies for Generic Drugs Procedure for Conducting Stability Studies on Generic Drug Products 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on generic drug products to evaluate their shelf life and storage conditions under various environmental factors such as temperature, humidity, and…
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How to Prepare a Stability Protocol in Accordance with ICH Q1A(R2) Developing a Stability Protocol Following ICH Q1A(R2) Guidelines Introduction A well-defined stability protocol is critical for conducting stability studies that are compliant with regulatory requirements. The ICH Q1A(R2) guidelines provide a comprehensive framework for the stability testing of drug substances and products, including the…
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SOP for Monitoring Microbial Stability in Drug Products Procedure for Assessing Microbial Stability in Pharmaceutical Products 1) Purpose The purpose of this SOP is to provide a standardized procedure for monitoring the microbial stability of drug products over time to ensure they remain free from harmful microorganisms throughout their shelf life. 2) Scope This SOP…
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How to Conduct Stability Testing for Drug Products Under ASEAN Guidelines Guidelines for Stability Testing of Drug Products in ASEAN Countries Introduction Stability testing is essential to ensure that drug products maintain their quality, safety, and efficacy throughout their shelf life. The Association of Southeast Asian Nations (ASEAN) has established specific guidelines for stability testing…
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How to Perform Stability Studies Following EMA (European Medicines Agency) Guidelines Conducting Stability Studies in Compliance with EMA Requirements Introduction Stability studies are a fundamental aspect of the pharmaceutical development process, ensuring that a product maintains its intended quality, safety, and efficacy throughout its shelf life. The European Medicines Agency (EMA) has established specific guidelines…
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How to Report Stability Data in Common Technical Document (CTD) Format Reporting Stability Data in CTD Format: A Comprehensive Guide Introduction Stability data is a crucial component of regulatory submissions for pharmaceutical products, providing evidence of the product’s quality, safety, and efficacy over its shelf life. The Common Technical Document (CTD) format, developed by the…
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SOP for Conducting Stability Studies for Liquid Dosage Forms Procedure for Performing Stability Studies on Liquid Dosage Forms 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on liquid dosage forms to evaluate their shelf life and storage conditions under various environmental factors such as temperature, humidity,…
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How to Conduct Bracketing and Matrixing Studies per ICH Q1D Implementing Bracketing and Matrixing Designs According to ICH Q1D Guidelines Introduction Bracketing and matrixing are two scientifically sound approaches that can be employed in stability testing to reduce the number of stability tests required while still ensuring product quality over time. The ICH Q1D guideline…
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How to Ensure Compliance with US FDA Stability Testing Requirements Achieving Compliance with US FDA Stability Testing Standards Introduction Stability testing is a critical requirement for ensuring that pharmaceutical products maintain their quality, safety, and efficacy throughout their shelf life. The US Food and Drug Administration (FDA) mandates specific stability testing guidelines under the Code…
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