Tag: Drug substance stability

Regulatory Guidelines for Stability Testing of APIs in Emerging Markets Comprehensive Guide to Regulatory Guidelines for Stability Testing of APIs in Emerging Markets Introduction: The Importance of Stability Testing in Emerging Markets The pharmaceutical industry is witnessing significant growth in emerging markets, thanks to increasing healthcare demands and government investments. However, this expansion brings the…

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Regulatory Guidelines for Stability Testing of APIs in Emerging Markets Understanding Regulatory Guidelines for Stability Testing of APIs in Emerging Markets Introduction to Stability Testing in Emerging Markets The global pharmaceutical industry is expanding rapidly into emerging markets, offering new opportunities for drug manufacturers. However, navigating the regulatory landscape in these regions presents unique challenges,…

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Stability Challenges in Multi-Source APIs: Tools and Techniques Overcoming Stability Challenges in Multi-Source APIs with Effective Tools and Techniques Introduction to Multi-Source APIs in Pharma Stability Studies The pharmaceutical industry’s reliance on multi-source APIs (Active Pharmaceutical Ingredients) has grown due to globalization and the need for cost efficiency. Sourcing APIs from multiple manufacturers allows flexibility…

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API Stability Studies: Introduction What Are API Stability Studies? API Stability Studies involve the systematic evaluation of an Active Pharmaceutical Ingredient (API) to ensure it retains its quality, potency, and safety under various environmental conditions over time. These studies assess how factors like temperature, humidity, and light impact the stability and shelf life of APIs,…

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