Please use this identifier to cite or link to this item:
http://dspace.hmtu.edu.vn/handle/DHKTYTHD_123/12025| Title: | Guideline on good pharmacovigilance practices (GVP): Module VI – Collection, management and submission of reports of suspected adverse reactions to medicinal products (Rev 2) |
| Keywords: | pharmacovigilance practices |
| Issue Date: | 2017 |
| Publisher: | European Medicines Agency |
| Description: | Chính văn tài liệu |
| URI: | http://dspace.hmtu.edu.vn/handle/DHKTYTHD_123/12025 |
| Appears in Collections | Bộ môn Dược học |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Guideline on good pharmacovigilance practices.pdf Restricted Access | 2.07 MB | Adobe PDF |  Request Item |
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