Terms
Terms list
Terms list
| Name | Standards | |
|---|---|---|
| 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 |
| recruitment | SRPS EN ISO 14155:2021 | more |
| randomization | SRPS EN ISO 14155:2021 | more |
| quality control | SRPS EN ISO 14155:2021 | more |
| quality assurance | SRPS EN ISO 14155:2021 | more |
| principal investigator | SRPS EN ISO 14155:2021 | more |
| point of enrolment | SRPS EN ISO 14155:2021 | more |
| objective | SRPS EN ISO 14155:2021 | more |
| multicentre investigation | SRPS EN ISO 14155:2021 | more |
| monitoring | SRPS EN ISO 14155:2021 | more |
| medical device | SRPS EN ISO 20387:2021 | more |