Ensuring Drug Quality: Stability Testing for Safety and Efficacy
Received Date: Aug 01, 2025 / Published Date: Aug 29, 2025
Abstract
Drug stability testing is a critical process in pharmaceutical development, essential for ensuring drug safety, efficacy, and qual ity throughout the product lifecycle. This review synthesizes research on key aspects including degradation pathway elucidation, analytical method selection, and defining storage conditions to predict shelf life. The influence of packaging materials, polymor phism, photostability, and biopharmaceutical specific challenges are examined. Adherence to regulatory guidelines is stressed as fundamental for market approval. Advanced analytical techniques and accelerated testing methodologies are discussed for profiling degradation products and predicting long-term stability, emphasizing the comprehensive nature of stability assessments.
Citation: Lopez DM (2025) Ensuring Drug Quality: Stability Testing for Safety and Efficacy. Int J Res Dev Pharm L Sci 11: 287.
Copyright: 漏 2025 Dr. Maria Lopez This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted聽use, distribution and reproduction in any medium, provided the original author and source are credited.
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