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Pharma Stability: Insights, Guidelines, and Expertise

Tag: Drug stability studies,

SOP for Conducting Stability Studies for Vaccine Products

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SOP for Conducting Stability Studies for Vaccine Products Guidelines for Stability Studies of Vaccine Products 1) Purpose The purpose of this SOP is to outline the procedures and guidelines for conducting stability studies on vaccine products. These studies are critical to ensuring that vaccines maintain their efficacy, safety, and quality throughout their shelf life under…

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How to Analyze Stability Samples Using HPLC

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How to Analyze Stability Samples Using HPLC A Step-by-Step Guide to Analyzing Stability Samples Using HPLC Introduction High-Performance Liquid Chromatography (HPLC) is a widely used analytical technique in pharmaceutical stability testing, providing precise and reliable data on the stability of drug products. HPLC is particularly useful for identifying and quantifying degradation products, assessing potency, and…

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'How to' - Stability Studies

How to Perform Humidity Chamber Studies for Drug Products

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How to Perform Humidity Chamber Studies for Drug Products Conducting Humidity Chamber Studies for Drug Products: A Practical Guide Introduction Humidity is a key factor that can significantly affect the stability of drug products. Conducting humidity chamber studies allows pharmaceutical companies to assess how different levels of humidity impact the stability of a drug product…

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'How to' - Stability Studies

How to Conduct Photostability Testing of Drug Products

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How to Conduct Photostability Testing of Drug Products Step-by-Step Guide to Photostability Testing of Drug Products Introduction Photostability testing is a vital component of the stability testing process, aimed at understanding how exposure to light affects the stability of drug products. Light exposure can lead to the degradation of active pharmaceutical ingredients (APIs), resulting in…

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'How to' - Stability Studies

SOP for Evaluating the Stability of Nanoparticles in Drug Products

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SOP for Evaluating the Stability of Nanoparticles in Drug Products Procedure for Conducting Stability Studies on Nanoparticle Drug Products 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on nanoparticle drug products to evaluate their shelf life, efficacy, and safety under various environmental conditions such as temperature,…

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How to Determine the Impact of Temperature on Drug Stability

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How to Determine the Impact of Temperature on Drug Stability Evaluating Temperature’s Impact on Drug Stability: A Comprehensive Guide Introduction Temperature is one of the most critical factors affecting the stability of drug products. Understanding how temperature impacts a drug’s stability is essential for determining proper storage conditions and shelf life. Temperature fluctuations can accelerate…

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'How to' - Stability Studies

SOP for Conducting Stress Testing of Active Pharmaceutical Ingredients (APIs)

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SOP for Conducting Stress Testing of Active Pharmaceutical Ingredients (APIs) Procedure for Stress Testing of Active Pharmaceutical Ingredients (APIs) 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stress testing of Active Pharmaceutical Ingredients (APIs) to determine their intrinsic stability and to identify degradation products. This information is used…

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'How to' - Stability Studies

How to Establish Shelf Life Using Stability Data

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How to Establish Shelf Life Using Stability Data Determining Shelf Life with Stability Data: A Step-by-Step Guide Introduction Establishing the shelf life of drug products is a vital step in the pharmaceutical development process, ensuring that the products remain effective and safe for use over time. Shelf life is determined based on stability data, which…

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'How to' - Stability Studies

SOP for Conducting Stability Studies for Small Molecule Drugs

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SOP for Conducting Stability Studies for Small Molecule Drugs Procedure for Stability Studies on Small Molecule Drugs 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on small molecule drugs to evaluate their shelf life, potency, and safety under various environmental conditions such as temperature, humidity, and…

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How to Perform Real-Time Stability Testing for Drug Substances

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How to Perform Real-Time Stability Testing for Drug Substances Step-by-Step Guide to Real-Time Stability Testing of Drug Substances Introduction Real-time stability testing is a fundamental aspect of pharmaceutical development, providing the most accurate representation of a drug substance’s stability under normal storage conditions. This type of testing is essential for determining the shelf life and…

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  • Start Stability Protocol Design with ICH Q1A(R2) Guidance

    Tip: Always refer to ICH Q1A(R2) before designing a stability protocol to align with global regulatory expectations.
    Understanding the Tip: Why protocol design matters: Stability protocols define how long a pharmaceutical product remains safe and effective… Read more

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