Guideline on good pharmacovigilance practices (GVP): Module VI – Collection, management and submission of reports of suspected adverse reactions to medicinal products (Rev 2)

Please use this identifier to cite or link to this item: http://dspace.hmtu.edu.vn/handle/DHKTYTHD_123/12025

Full metadata record

DC Field	Value	Language
dc.date.accessioned	2022-04-27T01:52:00Z	-
dc.date.available	2022-04-27T01:52:00Z	-
dc.date.issued	2017	-
dc.identifier.uri	http://dspace.hmtu.edu.vn/handle/DHKTYTHD_123/12025	-
dc.description	Chính văn tài liệu	vi
dc.language.iso	en	vi
dc.publisher	European Medicines Agency	vi
dc.subject	pharmacovigilance	vi
dc.subject	practices	vi
dc.title	Guideline on good pharmacovigilance practices (GVP): Module VI – Collection, management and submission of reports of suspected adverse reactions to medicinal products (Rev 2)	vi
dc.type	Book	vi
Appears in Collections	Bộ môn Dược học

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Guideline on good pharmacovigilance practices.pdf Restricted Access		2.07 MB	Adobe PDF	Request Item