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: oxidative degradation impurities

Oxidative Degradation in Biopharmaceuticals: Risks and Mitigation

Posted on By

Oxidative Degradation in Biopharmaceuticals: Risks and Mitigation Managing Oxidative Degradation in Biopharmaceuticals: Risks and Mitigation Strategies Oxidative degradation is a prevalent and critical degradation pathway affecting the stability, efficacy, and safety of biopharmaceuticals. Proteins and peptides, due to their structural complexity and reactive amino acids, are particularly vulnerable to oxidation. Factors such as exposure to…

Read More “Oxidative Degradation in Biopharmaceuticals: Risks and Mitigation” »

Stability Testing for Biopharmaceuticals, Stability Testing Types

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
  • Match Stability Study Container-Closure Systems to Final Market Packaging

    Understanding the Tip: Why container-closure systems matter: Stability testing simulates how a drug product will behave over its shelf life.
    If the container-closure system used… Read more

Copyright © 2025 StabilityStudies.in.

Powered by PressBook WordPress theme