United States Pharmacopeia 39th Edition + National Formulary 34 English Print
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Cod produs/ISBN: 9783769265606.
Disponibilitate: Acest produs nu este momentan in stoc
Editura: United States Pharmacopeia (USP)
Limba: Engleza
Nr. pagini:
Coperta: Hardcover
Dimensiuni: 4 Volumes
An aparitie: 1 May 2016.
The USP 39-NF 34 standards will be deemed official by 1 May 2016. The USP is enforceable by the U.S. Food and Drug Administration for medicines manufactured and marketed in the United States.
The USP-NF is a combination of two official compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). The USP-NF contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics.
Includes a four-volume print main edition and two separate print supplements. Printed on thick, durable paper stock, for laboratory and manufacturing use. Each volume contains a complete table of contents and index. Shipped with a slipcase for easy access and storage.
Highlights & Features
More than 4,900 monographs with specifications for identity, strength, quality, purity, packaging, and labeling for substances and dosage forms.
More than 300 general chapters providing clear, step-by-step guidance for assays, tests, and procedures
Focus-specific charts and a combined index help you find the information you need
Helpful sections on reagents, indicators, and solutions, plus reference tables
Includes new General Chapter <800> Hazardous DrugsHandling in Healthcare Settings
Key Features
· 24 new and revised general chapters
· 87 new and revised monographs
· Focus-specific charts and a combined index help you find the information you need
· Helpful sections on reagents, indicators, and solutions, plus reference tables
The USP-NF offers convenient, comprehensive information for all phases of producing quality prescription, non-prescription, and compounded medicines; excipients; biologics; medical devices; and dietary supplements. It is essential for quality control, quality assurance, regulatory/compendial affairs, research and development, method development/analytical services, and corporate management.
Benefits & Applications
The USPNF offers convenient, comprehensive information for all phases of producing quality prescription, nonprescription, and compounded medicines; excipients; biologics; medical devices; and dietary supplements. It is essential for quality control, quality assurance, regulatory/compendial affairs, research and development, method development/analytical services, and corporate management. USPNF monographs and methods can help to
Ensure compliance with required U.S. quality standards
Work to world-recognized standards of precision and accuracy
Validate test results against proven benchmarks
Establish and validate in-house standard operating procedures, and specifications
Expedite new product development and approvals
A Valuable Reference for:
Scientists, professionals, and students working in or with:
Pharmaceuticalsprescription and nonprescription drugs
Biological and biotechnology products
Blood and blood products
Compounded preparations
Cosmetics
Dietary supplements
Excipients/other drug ingredients
Medical devices
Medical gases
Medical libraries
Pharmacies
Schools of medicine and pharmacy
Veterinary drugs
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An aparitie | 1 May 2016. |
Autor | United States Pharmacopeia (USP) |
Dimensiuni | 4 Volumes |
Editura | United States Pharmacopeia (USP) |
Format | Hardcover |
ISBN | 9783769265606. |
Limba | Engleza |
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