United States Pharmacopeia 39th Edition + National Formulary 34 English Print

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 Drugs—Handling 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 USP–NF 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. USP–NF 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: Pharmaceuticals—prescription 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
ebookshop

An aparitie	1 May 2016.
Autor	United States Pharmacopeia (USP)
Dimensiuni	4 Volumes
Editura	United States Pharmacopeia (USP)
Format	Hardcover
ISBN	9783769265606.
Limba	Engleza