| ARC-ST | Accreditation Review Council for Educational Programs in Surgical Technology |
|---|---|
| BLRC | Biomedical Library Review Committee |
| CAPERS | Computer Assisted Psychiatric Evaluation and Review System |
| CER | capital expenditure review; ceramide; conditioned emotional response; control electrical rhythm; cor... |
| CSR | central supply room; chart-stimulated recall [test]; Cheyne-Stokes respiration; continued stay revie... |
| institutional review board |
Also known in some countries as Ethics Review Board, or ERB. This is the scientific institution that is independent of the sponsor of the clinical trial that reviews and approves the study protocol on ethical treatment grounds and ensures that each participant enrolled in the trial has given their informed consent to participate. The IRB or ERB monitors the clinical trial from inception through completion.
Ãâó: www.lillytrials.com/docs/terminology.html
|
|---|---|
| institutional review board |
The IRB is charged with the responsibility of protecting the rights and welfare of human subjects involved in research.(See Human Subjects Office). http://www.ovpr.uga.edu/hso/guidelines.html#1
Ãâó: www.uga.edu/studentaffairs/assess/glossary.shtml
|
| institutional review board |
An Institutional Review Board (IRB) is an independent committee, comprised of individuals with diverse medical and non-medical backgrounds, that reviews and approves all study-related documents. An IRB approves protocols, Informed Consent forms, physician credentials and eligibility, and patient recruitment materials, such as print advertisements and public service announcements. ...
Ãâó: www.adventisthealthcare.com/WAH/services/cardiolog...
|
| institutional review board |
(IRB) for Research with Human Subjects - Reviews all proposed research projects that involve human subjects to assure that the rights of such subjects are protected, that adequate and informed consent for their participation is obtained, and that any possible benefits of the research are commensurate with the risks involved.
Ãâó: www.unlv.edu/depts/cas/glossary.htm
|
| institutional review board |
An independent body constituted of medical, scientific, and nonscientific members, whose responsibility it is to ensure the protection of the rights, safety, and well-being of human subjects involved in a trial by, among other things, reviewing, approving, and providing continuing review of trials, of protocols and amendments, and of the methods and material to be used in obtaining and documenting informed consent of the trial subjects.
Ãâó: trimanos.com/sys/terms.html
|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|