{"product_id":"compendium-of-drug-degradation-pathways-isbn-9781118832936","title":"Compendium of Drug Degradation Pathways","description":"\u003cp\u003e\u003cb\u003eProvides accurate and current information on drug degradation pathways\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eUnderstanding the degradation chemistry of pharmaceuticals is essential for drug formulation, stability testing, and regulatory compliance. \u003ci\u003eCompendium of Drug Degradation Pathways\u003c\/i\u003e presents a detailed analysis of the degradation pathways of 300+ widely used prescription and over-the-counter drugs, making it an indispensable reference for formulation and analytical scientists.\u003c\/p\u003e \u003cp\u003eDrug stability and impurity characterization play a critical role in pharmaceutical research and development, as degradation can impact efficacy, safety, and regulatory approval. Structured alphabetically, this compendium organizes degradation data into concise monographs, each summarizing a drug's chemical structure, degradation pathways, and stability considerations. By collating information from regulatory guidelines, scientific literature, and real-world drug formulations, Dr. Min Lin provides formulation chemists, regulatory scientists, and medicinal chemists with a clear understanding of degradation mechanisms under practical storage conditions.\u003c\/p\u003e \u003cul\u003e \u003cli\u003eProvides guidance on real-world drug degradation under long-term stability conditions\u003c\/li\u003e \u003cli\u003eSummarizes critical stability data for formulation and analytical scientists working in drug development and manufacturing\u003c\/li\u003e \u003cli\u003eOffers valuable insights into drug metabolism and in vivo degradation linked to potential toxicities\u003c\/li\u003e \u003cli\u003eUses a systematic and organized approach, grouping drugs by therapeutic categories and structural similarities\u003c\/li\u003e \u003cli\u003eIncludes a dedicated introduction on regulatory perspectives, impurity characterization, and stress testing methodologies\u003c\/li\u003e \u003c\/ul\u003e \u003cp\u003eWith increasing regulatory scrutiny on drug quality and safety, \u003ci\u003eCompendium of Drug Degradation Pathways\u003c\/i\u003e is a critical reference for professionals in pharmaceutical sciences, intellectual property law, and regulatory agencies reviewing Chemistry, Manufacturing, and Controls (CMC) sections of NDAs and ANDAs.\u003c\/p\u003e \u003cb\u003eMin Li\u003c\/b\u003e is currently the Chief Scientist of Huahai Pharmaceutical, Co., Ltd. responsible for analytical research and development. He received his PhD in Organic Chemistry from The Johns Hopkins University in 1991. Following postdoctoral research in medicinal chemistry, he has worked for several multinational pharmaceutical companies with increasing responsibilities, including Roche, Merck \u0026amp; Co., Inc., and Schering-Plough. Dr Li has led technical teams of senior-level scientists for various analytical and pharmaceutical manufacturing process investigations and troubleshooting, impurity research and qualification, study of drug degradation chemistry, analytical development, and support for new drug filing (NDA).","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47988957249765,"sku":"NP9781118832936","price":190.0,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9781118832936.jpg?v=1761782204","url":"https:\/\/k12savings.com\/products\/compendium-of-drug-degradation-pathways-isbn-9781118832936","provider":"K12savings","version":"1.0","type":"link"}