Terms
Terms list
Terms list
| Name | Standards | |
|---|---|---|
| examination | SRPS EN ISO 15189:2023 | more |
| consultant | SRPS EN ISO 15189:2023 | more |
| complaint | SRPS EN ISO 15189:2023 | more |
| competence | SRPS EN ISO 15189:2023 | more |
| commutability of a reference material | SRPS EN ISO 15189:2023 | more |
| clinical decision limit | SRPS EN ISO 15189:2023 | more |
| biological reference interval | SRPS EN ISO 15189:2023 | more |
| bias | SRPS EN ISO 15189:2023 | more |
| vulnerable subject | SRPS EN ISO 14155:2021 | more |
| verification | SRPS EN ISO 14155:2021 | more |
| validation | SRPS EN ISO 14155:2021 | more |
| use error | SRPS EN ISO 14155:2021 | more |
| unanticipated serious adverse device effect | SRPS EN ISO 14155:2021 | more |
| subject | SRPS EN ISO 14155:2021 | more |
| sponsor | SRPS EN ISO 14155:2021 | more |
| source document | SRPS EN ISO 14155:2021 | more |
| source data | SRPS EN ISO 14155:2021 | more |
| serious health threat | SRPS EN ISO 14155:2021 | more |
| serious adverse event | SRPS EN ISO 14155:2021 | more |
| serious adverse device effect | SRPS EN ISO 14155:2021 | more |