Catalog
| LDR | 02224cam a2200325ia 4500 | ||
| 001 | 0009304995▲ | ||
| 005 | 20180519121352▲ | ||
| 008 | 051214s2005 sz a b i100 0 eng d▲ | ||
| 020 | ▼a 9241209291▲ | ||
| 035 | ▼a (KERIS)BIB000010427195▲ | ||
| 040 | ▼aFQG▼cFQG▼dVP@▼dBAKER▼d224010▼d211009▼d221016▲ | ||
| 082 | 0 | 4 | ▼a 615.19 ▼2 21▲ |
| 090 | ▼a 615.19 ▼b W628w▲ | ||
| 111 | 2 | ▼a WHO Expert Committee on Specifications for Pharmaceutical Preparations▼n (39th :▼d 2004 :▼c Geneva, Switzerland)▲ | |
| 245 | 1 | 0 | ▼aWHO Expert Committee on Specifications for Pharmaceutical Preparations :▼bthirty-ninth report.▲ |
| 260 | ▼aGeneva:▼bWorld Health Organization,▼c2005.▲ | ||
| 300 | ▼avii, 142 p.:▼bill.;▼c24 cm.▲ | ||
| 440 | 0 | ▼aWHO technical report series,▼x0512-3054;▼v929▲ | |
| 500 | ▼a "WHO Expert Committee on Specifications for Pharmaceutical Preparations, Geneva, 25-29 October 2004"--P. v.▲ | ||
| 504 | ▼a Includes bibliographical references.▲ | ||
| 520 | ▼a This report discusses the monographs on antiretrovirals proposed for inclusion in The International Pharmacopoeia and specifications for radiopharmaceuticals, quality specifications for antituberculosis drugs and the revision of the monograph on artemisinin derivatives, as well as quality control of reference materials, good manufacturing practices, inspection, distribution and trade, and other aspects of quality assurance of pharmaceuticals, and regulatory issues. Several annexes include an amendment to good manufacturing practices: main principles regarding the requirement for the sampling of starting materials, guidelines on good manufacturing practices regarding water for pharmaceutical use, guidelines on the sampling of pharmaceutical products, and draft guidelines for registration of fixed-dose combination medicinal products.▲ | ||
| 650 | 0 | ▼a Drugs▼x Standards▼v congresses.▲ | |
| 650 | 0 | ▼a Pharmacopoeias▼v congresses.▲ | |
| 650 | 0 | ▼a Drugs▼x Quality control▼v congresses.▲ | |
| 650 | 0 | ▼a Pharmaceutical preparations▼x standards▲ | |
| 650 | 0 | ▼a Technology, Pharmaceutical▼x standards▲ | |
| 650 | 0 | ▼a Drug industry▲ | |
| 710 | 2 | ▼a World Health Organization.▲ | |
| 830 | 0 | ▼aTechnical report series (World Health Organization);▼v929.▲ | |
| 990 | ▼a 정영주▼b정영주▲ |
WHO Expert Committee on Specifications for Pharmaceutical Preparations :thirty-ninth report
Document Type
Foreign Book
Title
WHO Expert Committee on Specifications for Pharmaceutical Preparations : thirty-ninth report.
Corporate Name
Meeting name
WHO Expert Committee on Specifications for Pharmaceutical Preparations, (39th, : 2004, : Geneva, Switzerland)
Publication
Geneva : World Health Organization , 2005.
Physical Description
vii, 142 p. : ill. ; 24 cm.
Series Title
WHO technical report series , 0512-3054 ; 929
Technical report series (World Health Organization) ; 929.
Technical report series (World Health Organization) ; 929.
General Note
"WHO Expert Committee on Specifications for Pharmaceutical Preparations, Geneva, 25-29 October 2004"--P. v.
Bibliography Note
Includes bibliographical references.
Summary Note
This report discusses the monographs on antiretrovirals proposed for inclusion in The International Pharmacopoeia and specifications for radiopharmaceuticals, quality specifications for antituberculosis drugs and the revision of the monograph on artemisinin derivatives, as well as quality control of reference materials, good manufacturing practices, inspection, distribution and trade, and other aspects of quality assurance of pharmaceuticals, and regulatory issues. Several annexes include an amendment to good manufacturing practices: main principles regarding the requirement for the sampling of starting materials, guidelines on good manufacturing practices regarding water for pharmaceutical use, guidelines on the sampling of pharmaceutical products, and draft guidelines for registration of fixed-dose combination medicinal products.
Subject
ISBN
9241209291
Call Number
615.19 W628w
Items
RReservation
AAbsent
VPreservation
CLoan Campus
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