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WHO Expert Committee on Specifications for Pharmaceutical Preparations - WHO Technical Report Series, No. 885 - Thirty-fifth Report
(1999; 168 pages) [Spanish] Voir le document au format PDF
Table des matières
Afficher le documentWHO Expert Committee on Specifications for Pharmaceutical Preparations
Afficher le document1. Introduction
Ouvrir ce répertoire et afficher son contenu2. The international pharmacopoeia and related issues
Ouvrir ce répertoire et afficher son contenu3. International Chemical Reference Substances and Infrared Reference Spectra
Ouvrir ce répertoire et afficher son contenu4. Quality control - national laboratories
Ouvrir ce répertoire et afficher son contenu5. Good manufacturing practices
Ouvrir ce répertoire et afficher son contenu6. Quality systems and inspection
Ouvrir ce répertoire et afficher son contenu7. Other quality assurance topics
Ouvrir ce répertoire et afficher son contenu8. Nomenclature and terminology
Ouvrir ce répertoire et afficher son contenu9. Legal aspects of pharmaceuticals
Ouvrir ce répertoire et afficher son contenu10. Regulatory issues
Ouvrir ce répertoire et afficher son contenu11. Training activities
Afficher le document12. Pharmaceuticals contaminated with diethylene glycol
Afficher le documentAcknowledgements
Afficher le documentReferences
Afficher le documentAnnex 1. List of available International Chemical Reference Substances1
Afficher le documentAnnex 2. List of available International Infrared Reference Spectra1
Ouvrir ce répertoire et afficher son contenuAnnex 3. General guidelines for the establishment, maintenance and distribution of chemical reference substances
Ouvrir ce répertoire et afficher son contenuAnnex 4. Good manufacturing practices: authorized person - role, functions and training
Ouvrir ce répertoire et afficher son contenuAnnex 5. Good manufacturing practices: supplementary guidelines for the manufacture of pharmaceutical excipients
Ouvrir ce répertoire et afficher son contenuAnnex 6. Guidelines for inspection of drug distribution channels
Afficher le documentAnnex 7. Good pharmacy practice in community and hospital pharmacy settings
Ouvrir ce répertoire et afficher son contenuAnnex 8. National drug regulatory legislation: guiding principles for small drug regulatory authorities
Ouvrir ce répertoire et afficher son contenuAnnex 9. Provisional guidelines for developing training programmes: inspection and examination of counterfeit pharmaceuticals
Afficher le documentWorld Health Organization Technical Report Series
Afficher le documentSelected WHO Publications of Related Interest
Afficher le documentBack Cover
 

WHO Expert Committee on Specifications for Pharmaceutical Preparations - WHO Technical Report Series, No. 885 - Thirty-fifth Report

WHO Technical Report Series
885


World Health Organization
Geneva 1999

This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the World Health Organization

The World Health Organization was established in 1948 as a specialized agency of the United Nations serving as the directing and coordinating authority for international health matters and public health. One of WHO's constitutional functions is to provide objective and reliable information and advice in the field of human health, a responsibility that it fulfils in part through its extensive programme of publications.

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The WHO Technical Report Series makes available the findings of various international groups of experts that provide WHO with the latest scientific and technical advice on a broad range of medical and public health subjects. Members of such expert groups serve without remuneration in their personal capacities rather than as representatives of governments or other bodies; their views do not necessarily reflect the decisions or the stated policy of WHO. An annual subscription to this series, comprising about 10 such reports, costs Sw. fr. 132.- (Sw. fr. 92.40 in developing countries).

WHO Library Cataloguing in Publication Data

WHO Expert Committee on Specifications for Pharmaceutical Preparations (1997: Geneva, Switzerland) WHO Expert Committee on Specifications for Pharmaceutical Preparations: thirty-fifth report.

(WHO technical report series: 885)

1. Pharmaceutical preparations - standards 2. Drug industry 3. Quality control
4. Reference standards 5. Legislation, Drug 6. Guidelines I. Title II. Series

ISBN 92 4 120885 6 (Classification NLM: QV 771)
ISSN 0512-3054

The World Health Organization welcomes requests for permission to reproduce or translate its publications, in part or in full. Applications and enquiries should be addressed to the Office of Publications, World Health Organization, Geneva, Switzerland, which will be glad to provide the latest information on any changes made to the text, plans for new editions, and reprints and translations already available.

© World Health Organization 1999

Publications of the World Health Organization enjoy copyright protection in accordance with the provisions of Protocol 2 of the Universal Copyright Convention, All rights reserved.

The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of Its frontiers or boundaries.

The mention of specific companies or of certain manufacturers' products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters.

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