Clinical Trial Contact Information by Institution
Research Ethics and Compliance and Good Clinical Practice Training
More information regarding CITI training can be found at http://www.citiprogram.org. Check with your local IRB office for institutional requirements.
UNMC/UNO | 402.559.6463 | irbora@unmc.edu |
NDSU | 701.231.8995 | ndsu.irb@ndsu.edu |
UND | 701.777.4279 | und.irb@research.und.edu |
USD | 605.677.6184 | humansubjects@usd.edu |
UNK | 308.865.8843 | shannojj@unk.edu |
UNL | 402.472.6965 | irb@unl.edu |
BTNRH | 531-355-6700 | rebecca.cash@boystown.org |
UNMC/UNO | 402.559.6046 | iacucora@unmc.edu |
NDSU | 701.231.8114 | ndsu.iacuc@ndsu.edu |
UND | 701.777.4279 | und.iacuc@research.und.edu |
USD | 605-677-6184 | compliance@usd.edu |
UNK | 308-865-8545 | ranglackdh@unk.edu |
UNL | 402-472-4486 | iacuc@unl.edu |
BTNRH | 531-498-6584 | Barbara.morley@boystown.org |
Work with your sponsored programs office for assistance with budgeting and contract execution.
Scientific Review Committee
For studies at UNMC that involve oncology patients, and SRC application is required. Click here for information regarding policies, applications, and deadlines.
For studies at UNMC that involve oncology patients, and SRC application is required. Click here for information regarding policies, applications, and deadlines.
Clinicaltrials.gov Registration
Registration with clinicaltrials.gov is required for all applicable drug or device clinical trials. Click here for definitions of applicable clinical trials.