Pharma Stability: Insights, Guidelines, and Expertise
How to Conduct In-Use Stability Testing A Comprehensive Guide to In-Use Stability Testing of Drug Products Introduction In-use stability testing is essential for assessing how drug products maintain their stability, safety, and efficacy after being opened or reconstituted for use. This type of testing is crucial for products that are intended to be used over…
How to Determine the Shelf Life of Parenteral Products Determining Shelf Life for Parenteral Products: A Step-by-Step Guide Introduction Parenteral products, which are administered via injection, infusion, or implantation, require rigorous stability testing to ensure their safety, efficacy, and quality over time. Determining the shelf life of parenteral products is essential for setting appropriate expiration…
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How to Perform Long-Term Stability Testing A Comprehensive Guide to Performing Long-Term Stability Testing Introduction Long-term stability testing is a critical component of pharmaceutical development, providing essential data on how drug products behave under normal storage conditions over extended periods. This type of testing is crucial for determining the shelf life of a product and…
SOP for Performing Stability Studies for Modified Release Formulations Guidelines for Stability Testing of Modified Release Formulations 1) Purpose The purpose of this SOP is to provide a standardized approach for conducting stability studies for modified release formulations. These formulations are designed to release the active ingredient over a specific period, and their stability must…
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How to Assess the Effect of pH on Drug Stability Evaluating the Impact of pH on Drug Stability: A Step-by-Step Guide Introduction The pH of a drug product can significantly impact its stability, affecting both the chemical integrity of the active pharmaceutical ingredient (API) and the overall formulation. Understanding how pH influences drug stability is…
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How to Conduct Stability Testing for Solid Oral Dosage Forms A Step-by-Step Guide to Stability Testing for Solid Oral Dosage Forms Introduction Solid oral dosage forms, such as tablets and capsules, are among the most common forms of drug products. Conducting stability testing for solid oral dosage forms is essential to ensure that these products…
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How to Evaluate Stability of Combination Products Evaluating the Stability of Combination Products: A Step-by-Step Guide Introduction Combination products, which include two or more regulated components (e.g., drug-device, biologic-device), present unique challenges in stability testing due to the interaction between the different components. Evaluating the stability of combination products is essential to ensure that the…
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SOP for Conducting Stability Studies for Pediatric Formulations Guidelines for Stability Testing of Pediatric Formulations 1) Purpose The purpose of this SOP is to establish procedures for conducting stability studies for pediatric formulations. Stability studies are essential to ensure that pediatric formulations maintain their safety, efficacy, and quality throughout their intended shelf life under various…
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How to Perform Stability Studies for Generic Drugs Conducting Stability Studies for Generic Drugs: A Step-by-Step Guide Introduction Stability studies are a key requirement in the development and approval of generic drugs, ensuring that these products maintain their quality, safety, and efficacy throughout their shelf life. Conducting stability studies for generic drugs is essential for…
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How to Monitor Microbial Stability in Drug Products Monitoring Microbial Stability in Drug Products: A Comprehensive Guide Introduction Microbial stability is a critical aspect of ensuring the safety and efficacy of drug products, particularly those that are susceptible to microbial contamination. Monitoring microbial stability involves assessing the ability of a drug product to resist microbial…
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