|Title:||A WHO guide to good manufacturing practice (GMP) requirements. Pt. 3, Training|
Giosafatte, Eliseo di
Jahdav, Suresh S
World Health Organization. Dept. of Immunization, Vaccines and Biologicals
|Publisher:||Geneva : World Health Organization|
|Description:||"This guide is the result of cooperation between many colleagues and institutions. Ms Emma Uramis, BioCen, and Mr James Vesper, LearningPlus, prepared it for the Global Training Network, in collaboration with: Mr Dave McEachran, Aventis Pasteur Limited, Dr Benny Kaligis, BioFarma, Dr Eliseo Di Giosafatte, Chiron S.p.A., Dr Darryl Mills and Mr Geoff Lewis, CSL Limited, Ms Barbara Capone, GlaxoSmithKline, Dr Suresh S. Jahdav, Serum Institute of India Ltd, Dr Kaare Haslov and MSc Thomas Vadsholt"--Acknowledgements|
Parts 1 & 2 were published with the document numbers, WHO/VSQ/97.01 and WHO/VSQ/97.02
vii, 135 p.
|metadata.dc.subject.other:||Pharmaceuticals and Biologicals|
|Gov't Doc #:||WHO/IVB/05.24|
|Appears in Collections:||Technical Documents|
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