 |
 |
|
|
|
|
|
|
|
расширенный поиск | карта сайта |
|
|
|
PD CEN/TR 17223:2018 |  на печать | | Guidance on the relationship between EN ISO 13485:2016 (Medical devices. Quality management systems. Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation |
|
| | Библиография | Обозначение | PD CEN/TR 17223:2018 | | Заглавие на английском языке | Guidance on the relationship between EN ISO 13485:2016 (Medical devices. Quality management systems. Requirements for regulatory purposes) and European Medical Devices Regulation and In Vitro Diagnostic Medical Devices Regulation | | Количество страниц оригинала | 88 | |
| | |
|
|
|
| Цены |
| На языке оригинала |
0,00
|
|
|
|