Stressing the theory involved in formulating suspensions, emulsions, and colloidal drug products, this three-volume reference provides detailed information on specialized products, such as emulsions, liposomes, polymers, and polymeric pharmaceutical excipients. Written by over twenty-five international experts, it explains the requirements for conducting clinical research and obtaining approval for new drug products-furnishing a current, comprehensive review of U.S. drug regulations.
Stressing the theory involved in formulating suspensions, emulsions, and colloidal drug products, this three-volume reference provides detailed information on specialized products, such as emulsions, liposomes, polymers, and polymeric pharmaceutical excipients. Written by over twenty-five international experts, it explains the requirements for conducting clinical research and obtaining approval for new drug products-furnishing a current, comprehensive review of U.S. drug regulations.
Herbert A. Lieberman, Martin M. Rieger , Gilbert S. Banker
Inhaltsangabe
Part 1 Specialized dispersed system: specialized pharmaceutical emulsions liposomes polymeric dispersions as drug carriers aqueous polymer dispersions as film formers biodegradable nanoparticles of poly(lactic acid) and poly(lactic-co-glycolic acid) for parenteral administration aqueous polymeric dispersions polymeric pharmaceutical excipients. Part 2 Equipment, processing, quality assurance, validation, regulation: a practical guide to equipment selection and operating techniques set-up to manufacturing scale-up of dispersed parenteral dosage form quality assurance validation of disperse systems drug regulatory affairs.
Part 1 Specialized dispersed system: specialized pharmaceutical emulsions liposomes polymeric dispersions as drug carriers aqueous polymer dispersions as film formers biodegradable nanoparticles of poly(lactic acid) and poly(lactic-co-glycolic acid) for parenteral administration aqueous polymeric dispersions polymeric pharmaceutical excipients. Part 2 Equipment, processing, quality assurance, validation, regulation: a practical guide to equipment selection and operating techniques set-up to manufacturing scale-up of dispersed parenteral dosage form quality assurance validation of disperse systems drug regulatory affairs.
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