Medical Technology Assessment Directory

Medical Technology Assessment Directory
Author: Institute of Medicine
Publisher: National Academies Press
Total Pages: 709
Release: 1988-02-01
Genre: Medical
ISBN: 0309038294

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For 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.

Usp38-Nf33

Usp38-Nf33
Author: United States Pharmacopeial Convention
Publisher:
Total Pages:
Release: 2014-11-01
Genre: Medicine
ISBN: 9781936424320

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USP 33 NF 28

USP 33 NF 28
Author: United States Pharmacopeial Convention
Publisher:
Total Pages: 668
Release: 2010
Genre:
ISBN: 9781889788883

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Usp35-Nf30

Usp35-Nf30
Author: United States Pharmacopeial Convention
Publisher: U.S. Pharmacopeia
Total Pages: 0
Release: 2011-11
Genre: Catalogs, Drug
ISBN: 9781936424009

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The 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).

The United States Pharmacopeia

The United States Pharmacopeia
Author: United States Pharmacopeial Convention
Publisher: U.S. Pharmacopeia
Total Pages: 0
Release: 2013
Genre: Medicine
ISBN: 9781936424221

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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. Learn more about the USP–NF and how it is developed.

The International Pharmacopoeia

The International Pharmacopoeia
Author: World Health Organization
Publisher: World Health Organization
Total Pages: 1526
Release: 2006
Genre: Medical
ISBN: 924156301X

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The International Pharmacopoeia contains a collection of recommended methods for analysis and quality specifications for pharmaceutical substances, excipients and products. This new edition consolidates the texts of the five separate volumes of the third edition and includes new monographs for antiretroviral substances (didanosine, indinavir sulfate, nelfinavir mesilate, nevirapine, ritonavir, saquinovir, and saquinovir mesilate) adopted by the WHO Expert Committee on Specifications for Pharmaceutical Preparations in October 2004. It includes some additions and amendments to the general notices of the Pharmacopoeia, as well as some changes to its layout and format. Volume one contains monographs for pharmaceutical substances A to O and the General Notices; and volume two contains monographs for pharmaceutical substances P to Z, together with those for dosage forms and radiopharmaceutical preparations, the methods of analysis and reagents.

Usp39-Nf34

Usp39-Nf34
Author: United States Pharmacopeial Convention
Publisher:
Total Pages:
Release: 2015-11-01
Genre:
ISBN: 9781936424443

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Botanical Dietary Supplements:

Botanical Dietary Supplements:
Author: Gail B. Mahady
Publisher: CRC Press
Total Pages: 288
Release: 2001-06-01
Genre: Science
ISBN: 9789026518553

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This volume provides reviews and details of the quality, safety and efficacy for some of the top-selling botanicals worldwide, including black cohosh, chamomile, comfrey, echinacea, garlic, ginkgo, ginseng, kava, milk thistle, St John's wort and valerian. The work was written based on a systematic review of the scientific literature from 1975-2000.;Each review includes a brief introduction, a section on quality including a definition of the crude drug, geographical distribution, and a listing of the major chemical constituents. The safety and efficacy sections summarize the medical uses, pharmacology, contraindications, warnings, precautions, adverse reactions, dose and dosage forms. The safety and efficacy sections were written for a busy health-care professional, and should enable one to ascertain which clinical uses are supported by clinical data, without having to read through all the pharmacology. Each chapter is fully referenced, enabling the reader to access further information when necessary.

Drugs on the Page

Drugs on the Page
Author: Matthew James Crawford
Publisher: University of Pittsburgh Press
Total Pages: 373
Release: 2019-05-15
Genre: Science
ISBN: 0822986833

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In the early modern Atlantic World, pharmacopoeias—official lists of medicaments and medicinal preparations published by municipal, national, or imperial governments—organized the world of healing goods, giving rise to new and valuable medical commodities such as cinchona bark, guaiacum, and ipecac. Pharmacopoeias and related texts, developed by governments and official medical bodies as a means to standardize therapeutic practice, were particularly important to scientific and colonial enterprises. They served, in part, as tools for making sense of encounters with a diversity of peoples, places, and things provoked by the commercial and colonial expansion of early modern Europe. Drugs on the Page explores practices of recording, organizing, and transmitting information about medicinal substances by artisans, colonial officials, indigenous peoples, and others who, unlike European pharmacists and physicians, rarely had a recognized role in the production of official texts and medicines. Drawing on examples across various national and imperial contexts, contributors to this volume offer new and valuable insights into the entangled histories of knowledge resulting from interactions and negotiations between Europeans, Africans, and Native Americans from 1500 to 1850.