Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/23689| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Koevski M. | en_US |
| dc.contributor.author | Tonikj ribarska, Jasmina | en_US |
| dc.contributor.author | Anchevska netkovska, Katerina | en_US |
| dc.contributor.author | Trajkovikj jolevska, Suzana | en_US |
| dc.date.accessioned | 2022-10-20T11:56:05Z | - |
| dc.date.available | 2022-10-20T11:56:05Z | - |
| dc.date.issued | 2018-10 | - |
| dc.identifier.uri | http://hdl.handle.net/20.500.12188/23689 | - |
| dc.language.iso | en | en_US |
| dc.title | New EU medical devices regulations – key challenges related to quality and safety of medical devices | en_US |
| dc.type | Article | en_US |
| dc.relation.conference | VII Serbian Congress of pharmacy with international participation | en_US |
| item.fulltext | No Fulltext | - |
| item.grantfulltext | none | - |
| crisitem.author.dept | Faculty of Pharmacy | - |
| crisitem.author.dept | Faculty of Pharmacy | - |
| crisitem.author.dept | Faculty of Pharmacy | - |
| Appears in Collections: | Faculty of Pharmacy: Conference papers | |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.