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Pharma Stability: Insights, Guidelines, and Expertise

Tag: Stability study design

Leveraging Shelf-Life Studies for Regulatory Approvals

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Leveraging Shelf-Life Studies for Regulatory Approvals Expert Guide to Using Shelf-Life Studies for Regulatory Success Introduction to Shelf-Life Studies Shelf-life studies are a cornerstone of pharmaceutical development, providing critical data to ensure that drug products remain safe, effective, and high-quality throughout their intended use. By assessing how environmental factors like temperature, humidity, and light impact…

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Types of Stability Studies

Addressing Excursions in Long-Term Stability Studies for APIs

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Addressing Excursions in Long-Term Stability Studies for APIs Effective Strategies to Address Excursions in Long-Term Stability Studies for APIs Introduction to Stability Studies for APIs Long-term stability studies are a critical component of pharmaceutical development, ensuring that Active Pharmaceutical Ingredients (APIs) maintain their quality, safety, and efficacy over their intended shelf life. However, excursions—temporary deviations…

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Stability Studies - API

Accelerated Stability Testing for Vaccines: Challenges and Solutions

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Accelerated Stability Testing for Vaccines: Challenges and Solutions Exploring Accelerated Stability Testing for Vaccines: Challenges and Emerging Solutions Introduction to Accelerated Stability Testing for Vaccines Vaccines are critical in preventing infectious diseases, but their development and distribution require stringent quality control processes. One essential aspect of ensuring vaccine safety and efficacy is stability testing. Among…

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Types of Stability Studies

PIC/S Guidelines: Harmonizing Global Stability Testing Practices

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PIC/S Guidelines: Harmonizing Global Stability Testing Practices Harmonizing Global Stability Testing Practices: The Role of PIC/S Guidelines Introduction In the pharmaceutical industry, stability testing ensures that products maintain their safety, quality, and efficacy throughout their shelf life. The Pharmaceutical Inspection Co-operation Scheme (PIC/S) plays a critical role in harmonizing these testing practices globally. By providing…

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Regulatory Guidelines

Freeze-Drying Techniques for Stability in API Formulations

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Freeze-Drying Techniques for Stability in API Formulations Comprehensive Guide to Freeze-Drying Techniques for Stability in API Formulations Introduction to Freeze-Drying in API Formulations Freeze-drying, or lyophilization, is a widely used process in pharmaceutical manufacturing to enhance the stability of Active Pharmaceutical Ingredients (APIs). This technique involves removing water from APIs and formulations under low-temperature and…

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Stability Studies - API

Designing Stability Studies for Orally Inhaled and Nasal Drug Products (OINDPs)

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Designing Stability Studies for Orally Inhaled and Nasal Drug Products (OINDPs) Expert Guide to Stability Studies for Orally Inhaled and Nasal Drug Products Introduction to Stability Testing for OINDPs Orally inhaled and nasal drug products (OINDPs) are complex pharmaceutical formulations designed to deliver medication directly to the respiratory system or nasal passages. These products include…

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Types of Stability Studies

TGA Guidelines for Stability Testing in Pharmaceuticals: An Overview

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TGA Guidelines for Stability Testing in Pharmaceuticals: An Overview Comprehensive Overview of TGA Stability Testing Guidelines in Pharmaceuticals Introduction Stability testing is a vital aspect of pharmaceutical product development, ensuring that medicines remain effective, safe, and of high quality throughout their shelf life. In Australia, the Therapeutic Goods Administration (TGA) oversees the regulation of stability…

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Regulatory Guidelines

Regulatory Trends in Stability Testing for APIs in Global Markets

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Regulatory Trends in Stability Testing for APIs in Global Markets Exploring Regulatory Trends in Stability Testing for APIs in Global Markets Introduction to Stability Testing in Global Markets Stability testing of Active Pharmaceutical Ingredients (APIs) is a cornerstone of pharmaceutical development and regulatory compliance. As global markets evolve, regulatory agencies are implementing updated guidelines and…

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Stability Studies - API

Freeze-Thaw Cycles and Their Impact on Pharmaceutical Stability

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Freeze-Thaw Cycles and Their Impact on Pharmaceutical Stability Exploring the Impact of Freeze-Thaw Cycles on Pharmaceutical Stability Introduction to Freeze-Thaw Cycles in Pharmaceutical Stability Pharmaceutical products often encounter temperature fluctuations during storage and transportation, particularly during distribution in global markets. Freeze-thaw cycles, which involve repeated freezing and thawing, can significantly impact the stability, safety, and…

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Types of Stability Studies

Advanced Tools for Real-Time Monitoring in API Stability Studies

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Advanced Tools for Real-Time Monitoring in API Stability Studies Exploring Advanced Tools for Real-Time Monitoring in API Stability Studies Introduction to Real-Time Monitoring in Stability Studies Real-time monitoring is revolutionizing API stability studies, providing dynamic insights into how Active Pharmaceutical Ingredients (APIs) respond to environmental factors such as temperature, humidity, and light. Unlike traditional stability…

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Stability Studies - API

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Quick Guide

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  • Stability Testing Types
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    • Real-Time and Accelerated Stability Studies
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    • Freeze-Thaw and Thermal Cycling Studies
    • Photostability and Oxidative Stability Studies
    • Stability Testing for Biopharmaceuticals
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  • Conduct Freeze-Thaw Studies for Biologics and Cold Chain Pharmaceuticals

    Understanding the Tip: What are freeze-thaw studies and their purpose: Freeze-thaw studies simulate repeated cycles of freezing and thawing that cold chain pharmaceutical products may… Read more

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