dc.contributor.author | Chaloner-Larsson, Gillian | en |
dc.contributor.author | Anderson, Roger | en |
dc.contributor.author | Egan, Anik | en |
dc.contributor.author | Da Fonseca Costa Filho, Manoel Antonio | en |
dc.contributor.author | Gomez Herrera, Jorge F | en |
dc.contributor.author | World Health Organization. Vaccine Supply and Quality Unit | en |
dc.coverage.spatial | Geneva | |
dc.date.accessioned | 2012-06-16T23:48:52Z | |
dc.date.available | 2012-06-16T23:48:52Z | |
dc.date.created | 1999 | en |
dc.date.issued | 1999 | en |
dc.identifier.govdoc | WHO/VSQ/97.01 | en |
dc.identifier.govdoc | WHO/VSQ/97.02 | en |
dc.identifier.uri | https://iris.who.int/handle/10665/64465 | |
dc.description | WHO/VSQ/97.01 | en |
dc.description | WHO/VSQ/97.02 | en |
dc.description | 2pts. in 2v. | en |
dc.language.iso | en | en |
dc.language.iso | ru | en |
dc.language.iso | es | en |
dc.publisher | World Health Organization | |
dc.publisher | World Health Organization | |
dc.subject.mesh | Vaccines | en |
dc.subject.mesh | Drug Industry | en |
dc.subject.mesh | Quality Control | en |
dc.subject.mesh | Guideline | en |
dc.subject.other | Pharmaceuticals and Biologicals | en |
dc.title | A WHO guide to good manufacturing practice (GMP) requirements / written by Gillian Chaloner-Larsson, Roger Anderson, Anik Egan; in collaboration with Manoel Antonio da Fonseca Costa Filho, Jorge F. Gomez Herrera | en |
dc.subject.meshqualifier | standards | en |
dc.subject.meshqualifier | methods | en |
who.relation.languageVersion | 10665/89219 | |
who.relation.languageVersion | 10665/89220 | |
who.relation.languageVersion | 10665/68527 | en |
who.relation.languageVersion | 10665/64975 | en |