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内容説明
?The Encyclopaedia of Pharmaceutical Technology? presents authoritative and contemporary articles on all aspects of drug development， dosage forms， manufacturing， and regulation - enabling the specialist and novice alike to keep abreast of developments in this rapidly evolving and highly competitive field. This is a dependable reference tool and a solid investment for years to come - it maintains currency through its supplements [Volume 18/Supplement 1: Published November， 1998]. The Encyclopaedia contains interdisciplinary contributions in a wide array of subjects， including: Drugs decomposition metabolism - pharmaceutical incompatibilities， pharmacokinetics physicochemical properties， preformulation stability; Drug Delivery Systems and Devices - Development and Manufacture analysis and controls bioavailability use of computerization formulation and processing alternatives national and international registration packaging patents process validation scale-up safety and efficacy stability standards; Post-Production and Practical Considerations governmental/industrial/professional organizations legal aspects national and international agencies patent life of drugs patient compliancea and much more!
Book Description
Now complete in 17 volumes， the Encyclopedia of Pharmaceutical Technology presents authoritative and contemporary articles on all aspects of drug development， dosage forms， manufacturing， and regulation;enabling the specialist and novice alike to keep abreast of developments in this rapidly evolving and highly competitive field. A dependable reference tool and a solid investment for years to come--maintaining currency through its supplements (Volume 18/Supplement 1 due to be published in the Fall， 1998)! The Encyclopedia contains interdisciplinary contributions in a wide array of subjects， including Drugs decomposition metabolism pharmaceutical incompatibilities pharmacokinetics physicochemical properties preformulation stability Drug Delivery Systems and Devices;Development and Manufacture analysis and controls bioavailability use of computerization formulation and processing alternatives national and international registration packaging patents process validation scale-up safety and efficacy stability standards Post-Production and Practical Considerations governmental/industrial/professional organizations legal aspects national and international agencies patent life of drugs patient compliance …and much， much more! Special Discount Offer New Subscribers ... save $415.00 off the subscription price of $3315.00! Purchase the entire 17-volume set for $2900.00 (only $171.00 per volume) offer expires 3/31/98 Missing volumes? For a limited time， complete your set at the special price of $171.00 per volume. offer expires 3/31/98