Amazon cover image
Image from Amazon.com

WHO expert committee on biological standardization / World Health Organization

Material type: TextTextPublication details: Geneva, Switzerland : World Health Organization, c2013Edition: Sixty-first reportDescription: xi, 384 pages ; 24 cmISBN:
  • 9789241209786
Subject(s): LOC classification:
  • HV 5825 .W46 2013
Contents:
1. Introduction -- 2. General -- 3. International Recommendations, Guidelines and other matters related to the manufacture and quality control of biologicals -- 4. International reference materials-vaccines and related substances -- 5. International reference materials-blood products and related substances -- 6. International reference materials-diagnostic reagents -- 7. International reference materials-biotherapeutics (other than blood products) -- 8. International reference materials-antibiotics -- References -- Annex 1 to Annex 7/
Summary: This report presents the recommendations of a WHO Expert Committee commissioned to coordinate activities leading to the adoption of international recommendations for the production and control of vaccines and other biologicals and the establishment of international biological reference materials. The report starts with a discussion of general issues brought to the attention of the Committee and provides information on the status and development of reference materials for various antibodies, antigens, blood products and related substances, cytokines, growth factors, endocrinological substances and in vitro diagnostic devices. The second part of the report, of particular relevance to manufacturers and national regulatory authorities, contains revised WHO recommendations for evaluation of animal-cell cultures as substrates for the manufacture of biological medicinal products, for production and control of hepatitis B vaccines and for production and control of yellow fever vaccines. New WHO guidelines on the independent lot release of vaccines are also included. Finally, there is an update to the procedure for the prequalification of vaccines. Also included are lists of recommendations, guidelines and other documents related to the manufacture and control of biological substances used in medicine, and of International Standards and Reference Reagents for biological substances.
Item type: Books
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Current library Home library Collection Call number Copy number Status Date due Barcode
Books Books National University - Manila LRC - Main General Circulation Pharmacy GC HV 5825 .W46 2013 (Browse shelf(Opens below)) c.1 Available NULIB000013675

Includes bibliographical references.

1. Introduction -- 2. General -- 3. International Recommendations, Guidelines and other matters related to the manufacture and quality control of biologicals -- 4. International reference materials-vaccines and related substances -- 5. International reference materials-blood products and related substances -- 6. International reference materials-diagnostic reagents -- 7. International reference materials-biotherapeutics (other than blood products) -- 8. International reference materials-antibiotics -- References -- Annex 1 to Annex 7/

This report presents the recommendations of a WHO Expert Committee commissioned to coordinate activities leading to the adoption of international recommendations for the production and control of vaccines and other biologicals and the establishment of international biological reference materials. The report starts with a discussion of general issues brought to the attention of the Committee and provides information on the status and development of reference materials for various antibodies, antigens, blood products and related substances, cytokines, growth factors, endocrinological substances and in vitro diagnostic devices. The second part of the report, of particular relevance to manufacturers and national regulatory authorities, contains revised WHO recommendations for evaluation of animal-cell cultures as substrates for the manufacture of biological medicinal products, for production and control of hepatitis B vaccines and for production and control of yellow fever vaccines. New WHO guidelines on the independent lot release of vaccines are also included. Finally, there is an update to the procedure for the prequalification of vaccines. Also included are lists of recommendations, guidelines and other documents related to the manufacture and control of biological substances used in medicine, and of International Standards and Reference Reagents for biological substances.

There are no comments on this title.

to post a comment.