ELIMINATING SIDE EFFECTS FROM PAPER FORMS CLINICAL RESEARCH'S TRANSITION TO ELECTRONIC ADVERSE EVENT LOGS.
Significance & Background: In clinical trials, it is essential to document key elements during each subject's visit to ensure comprehensive data collection. Adverse event (AE) logs represent a critical element of a research study as they allow study investigators, sponsors, and government regulatory...
| Publicado en: | Oncology Nursing Forum Vol. 53; no. 2; p. 53 |
|---|---|
| Autores principales: | , , , , , |
| Formato: | Journal Article |
| Publicado: |
Oncology Nursing Society
Mar2026
|
| Acceso en línea: | Ver este registro en EBSCOhost |