|
AE |
Adverse Event |
|---|---|
|
AEC |
Atomic Energy Commission |
|
ACHRE |
Advisory Committee on Human Radiation Experiments |
|
AMA |
American Medical Association |
|
CCRC |
Certified Clinical Research Coordinator |
|
CDC |
Centers for Disease Control and Prevention |
|
CFR |
Code of Federal Regulations |
|
CIOMS |
Council for International Organizations of Medical Sciences |
|
CRC |
Clinical Research Coordinator |
|
CRO |
Clinical Research Organization |
|
DAR |
Drug or Device Accountability Record |
|
DHHS |
Department of Health and Human Services |
|
FDA |
Food and Drug Administration |
|
FD&C Act |
Food, Drug and Cosmetic Act |
|
FERPA |
Family Educational Rights and Privacy Act |
|
GCP |
Good Clinical Practice |
|
ICH |
International Council on Harmonization |
|
IDE |
Investigational Device Exemption |
|
IND |
Investigational New Drug Application |
|
IRB |
Institutional Review Board |
|
MPA |
Multiple Project Assurance |
|
NBAC |
National Bioethics Advisory Commission |
|
NCI |
National Cancer Institute |
|
NDA |
New Drug Application |
|
NIH |
National Institutes of Health |
|
NIOSH |
National Institute for Occupational Safety & Health |
|
OHRP |
Office for Human Research Protections |
|
ORI |
Office of Research Integrity |
|
PHS |
Public Health Service |
|
PI |
Principal Investigator |
|
PMA |
Premarket Approval Application |
|
PPRA |
Protection of Pupil Rights Amendment |
|
TBI |
Total Body Irradiation |


