Coverart for item
The Resource WHO Expert Committee on Specifications for Pharmaceutical Preparations : thirty-seventh report, (electronic resource)

WHO Expert Committee on Specifications for Pharmaceutical Preparations : thirty-seventh report, (electronic resource)

Label
WHO Expert Committee on Specifications for Pharmaceutical Preparations : thirty-seventh report
Title
WHO Expert Committee on Specifications for Pharmaceutical Preparations
Title remainder
thirty-seventh report
Creator
Contributor
Subject
Genre
Language
eng
Member of
Cataloging source
CaPaEBR
Government publication
government publication level undetermined
Index
no index present
Literary form
non fiction
Nature of contents
standards specifications
http://bibfra.me/vocab/lite/organizationDate
2001 :
http://bibfra.me/vocab/lite/organizationName
WHO Expert Committee on Specifications for Pharmaceutical Preparations
http://library.link/vocab/relatedWorkOrContributorName
ebrary, Inc
Series statement
WHO technical report series,
Series volume
908
http://library.link/vocab/subjectName
  • Drugs
  • Drugs
  • Pharmaceutical industry
Label
WHO Expert Committee on Specifications for Pharmaceutical Preparations : thirty-seventh report, (electronic resource)
Instantiates
Publication
Color
multicolored
Contents
1. Introduction -- 2. General policy -- 3. Quality control--specifications and tests -- 4. Quality control--international reference materials -- 5. Quality control--national laboratories -- 6. Quality assurance--good manufacturing practices (GMP) -- 7. Quality assurance--inspection -- 8. Quality assurance--distribution and trade-related -- 9. Quality assurance--risk analysis -- 10. Quality assurance--drug supply -- 11. Quality assurance--storage -- 12. International Nonproprietary Names (INNs) Programme -- 13. Miscellaneous -- Annex 1. Recommendations on risk of transmitting animal spongiform encephalopathy agents via medicinal products -- Annex 2. The International Pharmacopoeia: revised concepts and future perspectives -- Annex 3. Guidelines on good manufacturing practices for radiopharmaceutical products -- Annex 4. Good manufacturing practices for pharmaceutial products: main prinicples -- Annex 5. Model certificate of good manufacturing practices -- Annex 6. Guidance on good manufacturing practices (GMP): inspection report -- Annex 7. Application of hazard analysis and critical control point (HACCP) method to pharmaceuticals -- Annex 8. Procedure for assessing the acceptability, in principle, of pharmaceutical products for purchase by United Nations agencies -- Annex 9. Guide to good storage practices for pharmaceuticals
Control code
ebr10040297
Dimensions
unknown
Extent
viii, 145 p
Form of item
electronic
Reproduction note
Electronic reproduction.
Specific material designation
remote
Label
WHO Expert Committee on Specifications for Pharmaceutical Preparations : thirty-seventh report, (electronic resource)
Publication
Color
multicolored
Contents
1. Introduction -- 2. General policy -- 3. Quality control--specifications and tests -- 4. Quality control--international reference materials -- 5. Quality control--national laboratories -- 6. Quality assurance--good manufacturing practices (GMP) -- 7. Quality assurance--inspection -- 8. Quality assurance--distribution and trade-related -- 9. Quality assurance--risk analysis -- 10. Quality assurance--drug supply -- 11. Quality assurance--storage -- 12. International Nonproprietary Names (INNs) Programme -- 13. Miscellaneous -- Annex 1. Recommendations on risk of transmitting animal spongiform encephalopathy agents via medicinal products -- Annex 2. The International Pharmacopoeia: revised concepts and future perspectives -- Annex 3. Guidelines on good manufacturing practices for radiopharmaceutical products -- Annex 4. Good manufacturing practices for pharmaceutial products: main prinicples -- Annex 5. Model certificate of good manufacturing practices -- Annex 6. Guidance on good manufacturing practices (GMP): inspection report -- Annex 7. Application of hazard analysis and critical control point (HACCP) method to pharmaceuticals -- Annex 8. Procedure for assessing the acceptability, in principle, of pharmaceutical products for purchase by United Nations agencies -- Annex 9. Guide to good storage practices for pharmaceuticals
Control code
ebr10040297
Dimensions
unknown
Extent
viii, 145 p
Form of item
electronic
Reproduction note
Electronic reproduction.
Specific material designation
remote

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