No hay productos en el carrito

2017 Usp40-Nf35 English Print Subscription
45-2400001-1u
1ª Edición Enero 2017
Inglés
Tapa dura
null pags
12000 gr
null x null x null cm
ISBN 9783800182947
Editorial varios
LIBRO IMPRESO
-5%
1326,00 €1259,70 €IVA incluido
1275,00 €1211,25 €IVA no incluido
Recíbelo en un plazo de
7 a 10 días
Description
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 othertherapeutics. 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. Learn more about the USP–NF and how it is developed.
A new edition with 2016 standards—USP 40–NF 35—becomes official August 1, 2017.
An official Spanish edition is available in print.
What's Inside USP 40–NF 35
- Index
Review and search the combined USP and NF index. - Admissions List. Find out what's new.
o USP 40–NF 35, First Supplement
- Annotated List. Learn what monographs, general chapters, reagents, and tables are affected by changes.
o USP 40–NF 35, First Supplement
Subscriber Resources
- Ordering Information
- Technical Services and Account Managers
- Currency Change Request
- Credit Application
- Authorized Distributors
Features
- More than 4,900 monographswithspecificationsforidentity, strength, quality, purity, packaging, and labelingforsubstances and dosageforms. View a sample USP–NF monograph.
- More than300 general chaptersprovidingclear, step-by-stepguidanceforassays, tests, and procedures
- Focus-specific charts and a combinedindexhelpyoufindtheinformationyouneed
- Helpfulsectionsonreagents, indicators, and solutions, plus referencetables
- Includes new General Chapter <800> HazardousDrugs—Handling in HealthcareSettings
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/compendialaffairs, research and development, method development/analytical services, and corporate management. USP–NF monographs and methods can help to
- Ensurecompliancewithrequired U.S. qualitystandards
- Work to world-recognizedstandards of precision and accuracy
- Validate test resultsagainstprovenbenchmarks
- Establish and validate in-house standard operatingprocedures, and specifications
- Expedite new productdevelopment and approvals
A Valuable Reference for
Scientists, professionals, and students working in or with
- Pharmaceuticals—prescription and nonprescriptiondrugs
- Biological and biotechnologyproducts
- Blood and bloodproducts
- Compoundedpreparations
- Cosmetics
- Dietarysupplements
- Excipients/otherdrugingredients
- Medical devices
- Medical gases
- Medical libraries
- Pharmacies
- Schools of medicine and pharmacy
- Veterinarydrugs
© 2025 Axón Librería S.L.
2.116.6