Clinical Trial (Oncology)
The following lists contain items and processes that may be completed to ensure compliance with the rules and regulations that govern clinical research. The below fees will be charged to the study account established for the protocol and shall be covered by the organization that is sponsoring or funding the clinical research:
|Administrative Start-Up||A one time, non-refundable fee.||$20,780|
|CTMS Set-Up||A one-time, non-refundable fee||$2,145|
|e-Regulatory||An Initial fee at start-up and annually thereafter, non-refundable||$1,700|
|Administrative Annual Fee||An annual, non-refundable fee||$6,530|
|Amendment Fee||A non-refundable fee charged for each sponsor required IRB amendment and sponsor prompted budget or contract amendment.
|Pre-Screening Fee||A non-refundable, quarterly fee, if applicable||Outpatient||$1,030|
|Training||Required additional protocol training for all personnel on DOA or 1572 through a sponsor system (per hour fee)||Study Personnel||$60|
|Sponsor/FDA Audit||Per day fee
|Local SAE Reporting||Per hour fee||$85|
|IRB Initial Review||A one-time fee||$3,900|
|IRB Continuation Review||An annual fee||$1,300|
|Administrative Close-Out||A one-time, non-refundable fee||$3,575|
|Archiving||A one-time, non-refundable fee
Email CTU for more information.