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Pharma Stability: Insights, Guidelines, and Expertise

Tag: Accelerated stability studies

TGA Stability Testing: A Detailed Look at Australian Requirements

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TGA Stability Testing: A Detailed Look at Australian Requirements Understanding TGA Stability Testing Guidelines: Australian Pharmaceutical Standards Introduction The Therapeutic Goods Administration (TGA) is Australia’s regulatory authority for therapeutic goods, ensuring that pharmaceutical products meet stringent safety, quality, and efficacy standards. Stability testing is a critical component of TGA regulatory requirements, providing evidence to support…

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Regulatory Guidelines

SOP for Performing Stability Studies for Sterile Products

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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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Stability Studies SOP

The Future of Stability Testing Regulations: Trends and Predictions

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The Future of Stability Testing Regulations: Trends and Predictions Exploring the Future of Stability Testing Regulations: Trends and Insights Introduction Stability testing regulations are at the core of pharmaceutical development, ensuring that products meet safety, quality, and efficacy standards throughout their lifecycle. As the industry evolves with advancements in science, technology, and sustainability, stability testing…

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Regulatory Guidelines

FDA and EMA Guidelines for Packaging Material Stability Testing

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FDA and EMA Guidelines for Packaging Material Stability Testing Understanding FDA and EMA Guidelines for Packaging Material Stability Testing Introduction Packaging plays a crucial role in maintaining the stability, quality, and efficacy of pharmaceutical products. Regulatory agencies like the FDA and EMA emphasize stringent guidelines for packaging material stability testing to ensure the integrity of…

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Regulatory Guidelines

SOP for Assessing Stability for Enzyme-Based Drugs

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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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Stability Studies SOP

Developing Stability Protocols for Multi-Regional Submissions

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Developing Stability Protocols for Multi-Regional Submissions Step-by-Step Guide to Developing Stability Protocols for Multi-Regional Submissions Introduction Pharmaceutical companies aiming for global market access must navigate diverse regulatory requirements across regions. Stability testing protocols for multi-regional submissions are essential to demonstrate product quality, safety, and efficacy under varying environmental conditions and regulatory frameworks. This guide provides…

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Regulatory Guidelines

ASEAN Stability Guidelines for APIs: Key Requirements Explained

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ASEAN Stability Guidelines for APIs: Key Requirements Explained Comprehensive Overview of ASEAN Stability Guidelines for APIs Introduction Active Pharmaceutical Ingredients (APIs) are the foundation of drug formulations, making their stability a critical factor in ensuring the safety, efficacy, and quality of pharmaceutical products. The ASEAN stability guidelines provide a harmonized framework for evaluating API stability…

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Regulatory Guidelines

SOP for Conducting Stability Studies for Drug Implants

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SOP for Conducting Stability Studies for Drug Implants Guidelines for Stability Testing of Drug Implants 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on drug implants. Stability testing is necessary to ensure that drug implants maintain their safety, efficacy, and quality under various storage conditions throughout…

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Stability Studies SOP

The Role of Stability Testing in Regulatory Approvals for Biologics

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The Role of Stability Testing in Regulatory Approvals for Biologics Expert Insights on Stability Testing for Biologics and Its Impact on Regulatory Approvals Introduction Biologics are complex pharmaceutical products derived from living organisms, including vaccines, monoclonal antibodies, and recombinant proteins. Stability testing for biologics is critical to ensure these products maintain their efficacy, safety, and…

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Regulatory Guidelines

SOP for Evaluating Stability for Drugs in Novel Packaging

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SOP for Evaluating Stability for Drugs in Novel Packaging Guidelines for Stability Testing of Drugs in Novel Packaging 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stability studies on drugs packaged in novel packaging materials. Stability testing ensures that the packaging maintains the drug’s safety, efficacy, and quality…

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Stability Studies SOP

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Quick Guide

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  • Prepare Expiry Justification Reports to Support Regulatory Queries and Renewals

    Understanding the Tip: What are expiry justification reports: Expiry justification reports are formal documents that summarize the rationale behind an assigned shelf life.
    They compile… Read more

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