Skip to content
  • Clinical Studies
  • Pharma Tips
  • Pharma GMP
  • Pharma SOP
  • Pharma Books
  • Schedule M
StabilityStudies.in

StabilityStudies.in

Pharma Stability: Insights, Guidelines, and Expertise

Tag: Drug product quality

Pharma Stability Studies Course – Conclusion

Posted on By

Congratulations on completing the Pharma Stability Studies course! Throughout this journey, you have delved into the intricacies of stability testing in the pharmaceutical industry, gaining a comprehensive understanding of its principles, practices, and applications. As we conclude, let’s reflect on the key takeaways from this course. Key Takeaways Understanding the importance of stability testing in…

Read More “Pharma Stability Studies Course – Conclusion” »

Stability Tutorials

Stability Reports

Posted on By

Stability reports are essential documents that summarize the results of stability studies conducted on pharmaceutical products. These reports provide critical information on the stability profile, shelf life, and storage recommendations for regulatory submissions, quality assurance, and manufacturing control. Key Components Stability reports typically include the following key components: 1. Objectives Define the objectives and scope…

Read More “Stability Reports” »

Stability Studies Blog

Are there guidelines for stability testing of pediatric and geriatric drug products?

Posted on By

Stability Testing Guidelines for Pediatric and Geriatric Drug Products Stability testing of drug products intended for pediatric and geriatric populations is essential to ensure that these specialized patient groups receive safe, effective, and high-quality medications. The unique physiological and dosage considerations for these populations require specific stability assessment approaches. In this discussion, I’ll outline the…

Read More “Are there guidelines for stability testing of pediatric and geriatric drug products?” »

Stability Studies FAQ

How can I address stability testing for orphan drug products with limited data?

Posted on By

Addressing Stability Testing for Orphan Drug Products with Limited Data Stability testing for orphan drug products with limited data presents unique challenges due to the scarcity of available information. However, regulatory agencies recognize the importance of ensuring the quality, safety, and efficacy of these specialized products. In this discussion, I’ll outline strategies for addressing stability…

Read More “How can I address stability testing for orphan drug products with limited data?” »

Stability Studies FAQ

What documentation should be included in stability study reports?

Posted on By

Documentation for Stability Study Reports Stability study reports are essential documents that provide a comprehensive overview of the study design, methods, results, and conclusions. These reports are submitted to regulatory authorities to demonstrate the quality, safety, and efficacy of pharmaceutical products over their intended shelf life. In this discussion, I’ll outline the key documentation that…

Read More “What documentation should be included in stability study reports?” »

Stability Studies FAQ

What role does stability testing play in the registration of new drug products?

Posted on By

Role of Stability Testing in New Drug Product Registration Stability testing plays a pivotal role in the registration process of new drug products, ensuring that pharmaceutical manufacturers provide robust scientific data to regulatory authorities. The data generated from stability studies serve as critical evidence of product quality, safety, and efficacy over time. In this discussion,…

Read More “What role does stability testing play in the registration of new drug products?” »

Stability Studies FAQ

ASEAN Guideline on Stability Study

Posted on By

Summary: ASEAN Guideline on Stability Study of Drug Products The ASEAN Guideline on Stability Study of Drug Products offers comprehensive recommendations for assessing the stability of pharmaceutical products across the ASEAN region. These guidelines are critical in ensuring that drug products maintain their quality, safety, and efficacy throughout their shelf-life. The ASEAN guideline aims to…

Read More “ASEAN Guideline on Stability Study” »

Regulatory Guidelines

Impurities: Guideline for Residual Solvents

Posted on By

Summary: ICH Q3C(R8) – Impurities: Guideline for Residual Solvents The ICH Q3C(R8) guideline provides essential recommendations for the control of residual solvents in pharmaceutical products. This guideline plays a crucial role in ensuring patient safety by limiting the exposure to potentially harmful solvents that may remain in the final drug product. The guidelines offer harmonized…

Read More “Impurities: Guideline for Residual Solvents” »

Regulatory Guidelines

FDA Guidance for Industry: Q1D

Posted on By

Summary: FDA Guidance Q1D – Bracketing and Matrixing Designs for Stability Testing The “FDA Guidance for Industry: Q1D Bracketing and Matrixing Designs for Stability Testing of Drug Substances and Products” provides valuable recommendations for optimizing stability testing protocols through the implementation of bracketing and matrixing designs. These approaches enable efficient testing by reducing the number…

Read More “FDA Guidance for Industry: Q1D” »

Regulatory Guidelines

ICH Q1B – Photostability Testing of New Drug Substances and Products

Posted on By

ICH Q1B – Guideline Summary ICH Q1B is a crucial regulatory guideline that focuses on the photostability testing of new drug substances and products. It addresses the potential effects of light exposure on pharmaceutical products, aiming to ensure their stability, safety, and efficacy throughout their shelf-life. Photostability testing is essential as light, particularly ultraviolet (UV)…

Read More “ICH Q1B – Photostability Testing of New Drug Substances and Products” »

Regulatory Guidelines

Posts pagination

Previous 1 … 15 16 17 18 Next

Quick Guide

  • Stability Tutorials
  • Stability Testing Types
    • Types of Stability Studies
    • Real-Time and Accelerated Stability Studies
    • Intermediate and Long-Term Stability Testing
    • Freeze-Thaw and Thermal Cycling Studies
    • Photostability and Oxidative Stability Studies
    • Stability Testing for Biopharmaceuticals
  • 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
Widget Image
  • Evaluate Both Chemical and Physical Stability in Pharmaceutical Studies

    Understanding the Tip: Why both stability types are critical: Stability isn’t just about potency retention (chemical stability); it’s also about how the product looks, feels,… Read more

Copyright © 2025 StabilityStudies.in.

Powered by PressBook WordPress theme