Tag: Stability System

How to Determine Degradation Pathways in Stability Studies Identifying Degradation Pathways in Stability Studies: A Comprehensive Guide Introduction Understanding the degradation pathways of drug products is a critical aspect of stability studies. Identifying how and why a drug product degrades under various conditions helps in developing stability-indicating methods, setting appropriate storage conditions, and ensuring the…

Read More “How to Determine Degradation Pathways in Stability Studies” »

How to Conduct Stability Studies for Biologics A Step-by-Step Guide to Conducting Stability Studies for Biologics Introduction Stability studies for biologics are critical in ensuring that these complex and sensitive products maintain their safety, efficacy, and quality throughout their shelf life. Unlike small molecule drugs, biologics are more prone to degradation due to their complex…

Read More “How to Conduct Stability Studies for Biologics” »

How to Interpret Stability Data for Regulatory Submissions Interpreting Stability Data for Regulatory Submissions: A Step-by-Step Guide Introduction Interpreting stability data is a crucial step in the pharmaceutical development process, particularly when preparing regulatory submissions. Stability data provides insights into the shelf life, storage conditions, and overall quality of drug products, making it a key…

Read More “How to Interpret Stability Data for Regulatory Submissions” »

How to Analyze Stability Samples Using HPLC A Step-by-Step Guide to Analyzing Stability Samples Using HPLC Introduction High-Performance Liquid Chromatography (HPLC) is a widely used analytical technique in pharmaceutical stability testing, providing precise and reliable data on the stability of drug products. HPLC is particularly useful for identifying and quantifying degradation products, assessing potency, and…

Read More “How to Analyze Stability Samples Using HPLC” »

How to Perform Humidity Chamber Studies for Drug Products Conducting Humidity Chamber Studies for Drug Products: A Practical Guide Introduction Humidity is a key factor that can significantly affect the stability of drug products. Conducting humidity chamber studies allows pharmaceutical companies to assess how different levels of humidity impact the stability of a drug product…

Read More “How to Perform Humidity Chamber Studies for Drug Products” »

How to Conduct Photostability Testing of Drug Products Step-by-Step Guide to Photostability Testing of Drug Products Introduction Photostability testing is a vital component of the stability testing process, aimed at understanding how exposure to light affects the stability of drug products. Light exposure can lead to the degradation of active pharmaceutical ingredients (APIs), resulting in…

Read More “How to Conduct Photostability Testing of Drug Products” »

How to Determine the Impact of Temperature on Drug Stability Evaluating Temperature’s Impact on Drug Stability: A Comprehensive Guide Introduction Temperature is one of the most critical factors affecting the stability of drug products. Understanding how temperature impacts a drug’s stability is essential for determining proper storage conditions and shelf life. Temperature fluctuations can accelerate…

Read More “How to Determine the Impact of Temperature on Drug Stability” »

SOP for Conducting Stress Testing of Active Pharmaceutical Ingredients (APIs) Procedure for Stress Testing of Active Pharmaceutical Ingredients (APIs) 1) Purpose The purpose of this SOP is to provide a standardized procedure for conducting stress testing of Active Pharmaceutical Ingredients (APIs) to determine their intrinsic stability and to identify degradation products. This information is used…

Read More “SOP for Conducting Stress Testing of Active Pharmaceutical Ingredients (APIs)” »