USP 41 - NF 36 The United States Pharmacopeia and National Formulary 2018
Main edition plus Supplements 1 and 2
Seiten
| Ausstattung: 5 Volumes
2017
Deutscher Apotheker Verlag
978-3-7692-7022-8 (ISBN)
Deutscher Apotheker Verlag
978-3-7692-7022-8 (ISBN)
Slipcase containing: Main work. 5 volume books. Hardcover. (November 2017). Including Supplement 1: (February 2018). Supplement 2: (June 2018)
The USP–NF is a combination of two compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). It contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics. The current version of USP–NF standards deemed official by USP are enforceable by the U.S. Food and Drug Administration for medicines manufactured and marketed in the United States.
USP 41–NF 36 —becomes official May 1, 2018.
An ISO certified Spanish translation (certified to ISO 17100:2015) of USP-NF compendial content is available in print as the Spanish edition.
Features
- More than 4,900 monographs with specifications for identity, strength, quality, purity, packaging, and labeling for substances and dosage forms.
- More than 350 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
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
The USP–NF is a combination of two compendia, the United States Pharmacopeia (USP) and the National Formulary (NF). It contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics. The current version of USP–NF standards deemed official by USP are enforceable by the U.S. Food and Drug Administration for medicines manufactured and marketed in the United States.
USP 41–NF 36 —becomes official May 1, 2018.
An ISO certified Spanish translation (certified to ISO 17100:2015) of USP-NF compendial content is available in print as the Spanish edition.
Features
- More than 4,900 monographs with specifications for identity, strength, quality, purity, packaging, and labeling for substances and dosage forms.
- More than 350 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
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
| Erscheinungsdatum | 22.11.2017 |
|---|---|
| Sprache | englisch |
| Gewicht | 18155 g |
| Einbandart | gebunden im Schuber |
| Themenwelt | Medizin / Pharmazie ► Pharmazie ► PTA / PKA |
| Schlagworte | 41 • Arzneibuch • Internationale Fachliteratur • Jahressubskription • Pharmazie • USA • USP • USP 41 • USP 41 - NF 36 Annual Subscription |
| ISBN-10 | 3-7692-7022-3 / 3769270223 |
| ISBN-13 | 978-3-7692-7022-8 / 9783769270228 |
| Zustand | Neuware |
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