Abstract
The stability of pharmaceutical preparations is a critical factor affecting their efficacy, safety, and shelf life. Variations in storage conditions, including temperature, humidity, and light exposure, can significantly influence the physical and chemical properties of these preparations. This paper investigates the stability of pharmaceutical preparations under varying storage conditions, focusing on the degradation rate of active ingredients, physical changes, and the impact of packaging materials. Data collected from accelerated and long-term stability studies are analyzed to provide recommendations for optimal storage conditions. Keywords: Pharmaceutical stability, degradation, storage conditions, accelerated stability testing, temperature, humidity, light exposure, active pharmaceutical ingredients (API), tablets, solutions, suspensions, packaging materials, shelf life, refrigeration, photodegradation
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