{"product_id":"pharmaceutical-dissolution-testing-bioavailability-and-bioequivalence","title":"Pharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence","description":"\u003cp\u003e\u003cb\u003eExplore the cutting-edge of dissolution testing in an authoritative, one-stop resource\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eIn \u003ci\u003ePharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence: Science, Applications, and Beyond\u003c\/i\u003e, distinguished pharmaceutical advisor and consultant Dr. Umesh Banakar delivers a comprehensive and up-to-date reference covering the established and emerging roles of dissolution testing in pharmaceutical drug development.\u003c\/p\u003e \u003cp\u003eAfter discussing the fundamentals of the subject, the included resources go on to explore common testing practices and methods, along with their associated challenges and issues, in the drug development life cycle.\u003c\/p\u003e \u003cp\u003eOver 19 chapters and 1100 references allow practicing scientists to fully understand the role of dissolution, apart from mere quality control. Readers will discover a wide range of topics, including automation, generic and biosimilar drug development, patents, and clinical safety.\u003c\/p\u003e \u003cp\u003eThis volume offers a one-stop resource for information otherwise scattered amongst several different regulatory regimes. It also includes:\u003c\/p\u003e \u003cul\u003e\n\u003cli\u003eA thorough introduction to the fundamentals and essential applications of pharmaceutical dissolution testing\u003c\/li\u003e\n\u003cli\u003eComprehensive explorations of the foundations and drug development applications of bioavailability and bioequivalence\u003c\/li\u003e\n\u003cli\u003ePractical discussions about solubility, dissolution, permeability, and classification systems in drug development\u003c\/li\u003e\n\u003cli\u003eIn-depth examinations of the mechanics of dissolution, including mathematical models and simulations\u003c\/li\u003e\n\u003cli\u003eAn elaborate assessment of biophysiologically relevant dissolution testing and IVIVCs, and their unique applications\u003c\/li\u003e\n\u003cli\u003eA complete understanding of the methods, requirements, and global regulatory expectations pertaining to dissolution testing of generic drug products\u003c\/li\u003e\n\u003c\/ul\u003e \u003cp\u003eIdeal for drug product development and formulation scientists, quality control and assurance professionals, and regulators, \u003ci\u003ePharmaceutical Dissolution Testing, Bioavailability, and Bioequivalence\u003c\/i\u003e is also the perfect resource for intellectual property assessors.\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Product","offer_id":54220977111384,"sku":"9781119634607","price":202.06,"currency_code":"EUR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0278\/1295\/4195\/files\/9781119634607__67654c964e279.jpg?v=1741159114","url":"https:\/\/agendabookshop.com\/products\/pharmaceutical-dissolution-testing-bioavailability-and-bioequivalence","provider":"Agenda Bookshop","version":"1.0","type":"link"}