Pharma Stability: Insights, Guidelines, and Expertise
How to Conduct Stability Studies for Topical Products in Compliance with US FDA and EMA Guidelines Conducting Stability Studies for Topical Products: US FDA and EMA Compliance Introduction Topical products, such as creams, ointments, and lotions, require specific stability studies to ensure their safety and efficacy over time. Compliance with US FDA and EMA guidelines…
How to Implement ICH Q9 for Risk Management in Stability Testing Applying ICH Q9 Principles for Effective Risk Management in Stability Testing Introduction ICH Q9 provides a systematic approach to risk management in the pharmaceutical industry, including stability testing. Effective implementation of ICH Q9 ensures that risks associated with stability testing are identified, evaluated, and…
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How to Conduct Stability Studies for Fixed-Dose Combination Products under Regulatory Guidelines Conducting Stability Studies for Fixed-Dose Combination Drugs: A Regulatory Approach Introduction Fixed-dose combination (FDC) products combine two or more active pharmaceutical ingredients (APIs) in a single dosage form. Conducting stability studies for these products is crucial to ensure their safety, efficacy, and quality…
How to Ensure Compliance with Global Stability Testing Requirements (US FDA, EMA, WHO) Ensuring Compliance with International Stability Testing Standards: A Comprehensive Guide Introduction Stability testing is a critical aspect of pharmaceutical development and quality assurance. Ensuring compliance with global stability testing requirements is essential for the approval, distribution, and maintenance of drug products in…
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