Tag: Drug degradation pathways

What are the implications of failing stability testing?

Implications of Failing Stability Testing Stability testing is a critical component of pharmaceutical development, ensuring that products maintain their quality and safety over time. However, when a pharmaceutical product fails stability testing, it can have significant implications for both the product and the manufacturer. In this discussion, I’ll delve into the key implications of failing…

Stability Studies FAQ

Are there specific temperature and humidity conditions for long-term stability studies?

Temperature and Humidity Conditions for Long-Term Stability Studies Long-term stability studies are essential to assess the quality, efficacy, and safety of pharmaceutical products over their intended shelf life. Proper temperature and humidity conditions play a critical role in maintaining product integrity throughout these studies. In this discussion, I’ll provide insights into the specific temperature and…

Stability Studies FAQ

Can stability testing be performed simultaneously on different drug strengths?

Simultaneous Stability Testing on Different Drug Strengths Absolutely, stability testing can indeed be performed simultaneously on different drug strengths. Conducting stability studies on various strengths of a pharmaceutical product can be an efficient and practical approach, especially when the strengths share the same formulation and packaging, with only the quantity of the active pharmaceutical ingredient…

Stability Studies FAQ

How are stability studies done for external preparations?

Stability Studies for External Preparations (Topical Products) Stability studies for external preparations, also known as topical products, involve assessing the physical, chemical, and microbiological attributes of products applied to the skin or mucous membranes. These studies ensure that the product remains safe, effective, and suitable for use throughout its intended shelf life. Conducting stability studies…

Stability Studies FAQ

How are stability studies performed?

Performing Stability Studies in Pharmaceuticals Stability studies in pharmaceuticals are carefully designed and executed to assess how a drug product’s quality, efficacy, and safety change over time and under various storage conditions. The process of performing stability studies involves several systematic steps: Study Design: Determine the study’s objectives, including the attributes to be tested, the…

Stability Studies FAQ