Usp39-Nf34
Author: United States Pharmacopeial Convention
Publisher:
Published: 2015-11-01
Total Pages:
ISBN-13: 9781936424443
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Usp38-Nf33
Author: United States Pharmacopeial Convention
Publisher:
Published: 2014-11-01
Total Pages:
ISBN-13: 9781936424320
DOWNLOAD EBOOKUsp35-Nf30
Author: United States Pharmacopeial Convention
Publisher: U.S. Pharmacopeia
Published: 2011-11
Total Pages: 0
ISBN-13: 9781936424009
DOWNLOAD EBOOKThe USP-NF is a combination of two official 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. USP-NF standards are enforceable by the U.S. Food and Drug Administration for medicines manufactured and marketed in the United States. Learn more about USP-NF. Highlights & Features: * More than 4,500 monographs with specifications for identity, strength, quality, purity, packaging, and labeling for substances and dosage forms. View a sample USP-NF monograph (100KB). * Over 230 General Chapters providing clear, step-by-step guidance for assays, tests, and procedures * Focus-specific charts and a combined index helps you find the information you need * Helpful sections on reagents, indicators, and solutions, plus reference tables * Published annually in an official English edition (print, CD, and new USB flash drive formats ) and an official Spanish edition (print).
USP 33 NF 28
Author: United States Pharmacopeial Convention
Publisher:
Published: 2010
Total Pages: 491
ISBN-13: 9781889788883
DOWNLOAD EBOOKCompounding Sterile Preparations
Author: E. Clyde Buchanan
Publisher: ASHP
Published: 2009-02-01
Total Pages: 497
ISBN-13: 1585283312
DOWNLOAD EBOOKEmpower your staff to improve safety, quality and compliance with the help of new guidelines and standards. We’ve updated every chapter of this popular review of the fundamentals of preparing sterile products in hospital, home-care, and community pharmacy settings to reflect the most recent revisions to USP . Included are the latest guidelines for the compounding process, quality assurance methods, and comprehensive coverage of all aspects of the dispensing process. Comprehensive documentation for the guidelines is included in the appendices.Chapters new to this edition focus on: Gap analysis and action plans Safe use of automatic compounding devices Cleaning and disinfecting Radiopharmaceuticals as CSPs Allergen extracts as CSPs.
The Chapter 800 Answer Book
Author: Patricia C. Kienle
Publisher:
Published: 2021-09-30
Total Pages: 0
ISBN-13: 9781585286294
DOWNLOAD EBOOK"Provides explanation of elements of USP Hazardous Drugs' Handling in Healthcare Settings and best practices to comply with the requirements and recommendations of the USP General Chapter"--Pref.
Medical Technology Assessment Directory
Author: Institute of Medicine
Publisher: National Academies Press
Published: 1988-02-01
Total Pages: 709
ISBN-13: 0309038294
DOWNLOAD EBOOKFor the first time, a single reference identifies medical technology assessment programs. A valuable guide to the field, this directory contains more than 60 profiles of programs that conduct and report on medical technology assessments. Each profile includes a listing of report citations for that program, and all the reports are indexed under major subject headings. Also included is a cross-listing of technology assessment report citations arranged by type of technology headings, brief descriptions of approximately 70 information sources of potential interest to technology assessors, and addresses and descriptions of 70 organizations with memberships, activities, publications, and other functions relevant to the medical technology assessment community.
Applied Pharmaceutics in Contemporary Compounding
Author: Robert P. Shrewsbury
Publisher: Morton Publishing Company
Published: 2015-01-01
Total Pages: 465
ISBN-13: 1617314196
DOWNLOAD EBOOKApplied Pharmaceutics in Contemporary Compounding, Third Edition is designed to convey a fundamental understanding of the principles and practices involved in both the development and the production of compounded dosage forms by applying pharmaceutical principles.
