Skip to content
  • Pharma Tips
  • Pharma GMP
  • Pharma SOP
  • Pharma Books
  • Schedule M

StabilityStudies.in

Pharma Stability: Insights, Guidelines, and Expertise

Tag: Stability testing

How to Conduct Stability Testing for Biosimilars in Compliance with WHO Guidelines

Posted on By

How to Conduct Stability Testing for Biosimilars in Compliance with WHO Guidelines Stability Testing for Biosimilars: A WHO Compliance Guide Introduction Biosimilars, which are biological products highly similar to their reference biologics, require comprehensive stability testing to ensure their safety, efficacy, and quality. The World Health Organization (WHO) provides guidelines for stability testing of biosimilars,…

Read More “How to Conduct Stability Testing for Biosimilars in Compliance with WHO Guidelines” »

'How to' - Stability Studies

How to Implement Stability Testing for Pediatric Formulations under US FDA and EMA Guidelines

Posted on By

How to Implement Stability Testing for Pediatric Formulations under US FDA and EMA Guidelines Stability Testing for Pediatric Formulations: A Regulatory Compliance Guide Introduction Pediatric formulations, which are specifically designed for children, require tailored stability testing to ensure their safety, efficacy, and quality. The US FDA and EMA have established guidelines that address the unique…

Read More “How to Implement Stability Testing for Pediatric Formulations under US FDA and EMA Guidelines” »

'How to' - Stability Studies

How to Conduct Stability Studies for Drug Products Stored at Subzero Temperatures under Regulatory Guidelines

Posted on By

How to Conduct Stability Studies for Drug Products Stored at Subzero Temperatures under Regulatory Guidelines Stability Studies for Drug Products at Subzero Temperatures: A Regulatory Guide Introduction Drug products stored at subzero temperatures, such as biologics, vaccines, and certain advanced therapies, require specific stability studies to ensure their safety, efficacy, and quality throughout their shelf…

Read More “How to Conduct Stability Studies for Drug Products Stored at Subzero Temperatures under Regulatory Guidelines” »

'How to' - Stability Studies

How to Implement Stability Testing for Polymorphic Drug Substances under Regulatory Guidelines

Posted on By

How to Implement Stability Testing for Polymorphic Drug Substances under Regulatory Guidelines Stability Testing for Polymorphic Drug Substances: Ensuring Regulatory Compliance Introduction Polymorphism in drug substances can significantly impact their stability, solubility, and bioavailability. Polymorphic forms of a drug may exhibit different physical and chemical properties, making stability testing essential to ensure the safety, efficacy,…

Read More “How to Implement Stability Testing for Polymorphic Drug Substances under Regulatory Guidelines” »

'How to' - Stability Studies

How to Address Stability Testing Requirements for Global Harmonization under ICH Guidelines

Posted on By

How to Address Stability Testing Requirements for Global Harmonization under ICH Guidelines Global Harmonization of Stability Testing: Navigating ICH Guidelines Introduction Global harmonization of stability testing is crucial for ensuring consistent quality, safety, and efficacy of pharmaceutical products across different markets. The International Council for Harmonisation (ICH) provides guidelines that unify stability testing requirements for…

Read More “How to Address Stability Testing Requirements for Global Harmonization under ICH Guidelines” »

'How to' - Stability Studies

SOP for Establishing Shelf Life Using Stability Data

Posted on By

SOP for Establishing Shelf Life Using Stability Data Procedure for Determining Shelf Life of Pharmaceuticals Using Stability Data 1) Purpose The purpose of this SOP is to provide guidelines for establishing the shelf life of pharmaceutical products using data obtained from stability studies. 2) Scope This SOP applies to all stability studies conducted to determine…

Read More “SOP for Establishing Shelf Life Using Stability Data” »

Stability Studies SOP

How to Implement Stability Testing for Orally Inhaled and Nasal Drug Products (OINDP) under FDA Guidelines

Posted on By

How to Implement Stability Testing for Orally Inhaled and Nasal Drug Products (OINDP) under FDA Guidelines Ensuring Stability of Orally Inhaled and Nasal Drug Products: A Guide to FDA Compliance Introduction Orally Inhaled and Nasal Drug Products (OINDPs), including inhalers, nasal sprays, and nebulizers, are complex formulations that require rigorous stability testing to ensure their…

Read More “How to Implement Stability Testing for Orally Inhaled and Nasal Drug Products (OINDP) under FDA Guidelines” »

'How to' - Stability Studies

How to Conduct Stability Studies for Controlled Drugs under Regulatory Guidelines

Posted on By

How to Conduct Stability Studies for Controlled Drugs under Regulatory Guidelines Ensuring Compliance in Stability Studies for Controlled Drugs Introduction Controlled drugs, including narcotics and psychotropics, require stringent stability testing to ensure their safety, efficacy, and quality throughout their shelf life. Regulatory authorities, such as the US DEA, FDA, and international bodies, provide specific guidelines…

Read More “How to Conduct Stability Studies for Controlled Drugs under Regulatory Guidelines” »

'How to' - Stability Studies

How to Address Stability Testing for Products under Emergency Use Authorization (EUA)

Posted on By

How to Address Stability Testing for Products under Emergency Use Authorization (EUA) Stability Testing for Products under EUA: Navigating Regulatory Requirements Introduction Emergency Use Authorization (EUA) allows for the use of medical products during public health emergencies, even when they have not completed the standard approval process. Stability testing for products under EUA is crucial…

Read More “How to Address Stability Testing for Products under Emergency Use Authorization (EUA)” »

'How to' - Stability Studies

SOP for Performing Real-Time Stability Testing for Drug Substances

Posted on By

SOP for Performing Real-Time Stability Testing for Drug Substances Standard Procedure for Conducting Real-Time Stability Testing on Drug Substances 1) Purpose The purpose of this SOP is to provide a structured procedure for conducting real-time stability testing of drug substances to ensure their safety, efficacy, and quality throughout their shelf life under recommended storage conditions….

Read More “SOP for Performing Real-Time Stability Testing for Drug Substances” »

Stability Studies SOP

Posts pagination

Previous 1 … 31 32 33 … 52 Next

Quick Guide

  • Stability Tutorials
  • Types of Stability Studies
  • Stability Studies SOP
  • ‘How to’ – Stability Studies
  • Regulatory Guidelines
  • Shelf Life and Expiry Dating
  • Stability Documentation
  • Stability Studies – API
  • Stability Studies Blog
  • Stability Studies FAQ
  • Packaging – Containers – Closers

    more

    Copyright © 2025 StabilityStudies.in.

    Powered by PressBook WordPress theme