16 Jul Units: TRU Service Requests
| Entry Date | Last | First | Email/Reply | View | Request Type | Institution / Organization | Department or Program | Preferred method(s) of contact | Phone | Full study name | Primary Investigator's full name | PI's email address | Requester phone number | Protocol | Lab Manual (if applicable) | Total number of study participants you wish to see on the CRC | Breakdown of requested services for each visit | Number of visits per study participant | Anticipated start date for CRC Services | Anticipated end date for CRC Services | Funding source | Full study name | Primary Investigator's full name | PI's email address | PI's primary phone | Key personnel who will interact with study participants | Study Protocol | IRB Approval Letter | Stamp-approved consent/assent forms | Is your study is being conducted under an IND or IDE? | Investigator’s Brochure or device manual (for all investigational products) | Is this a clinical trial? | Is this study investigator-initiated? | Entry ID | Source URL | User | User IP |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry Date | Last | First | Email/Reply | View | Request Type | Institution / Organization | Department or Program | Preferred method(s) of contact | Phone | Full study name | Primary Investigator's full name | PI's email address | Requester phone number | Protocol | Lab Manual (if applicable) | Total number of study participants you wish to see on the CRC | Breakdown of requested services for each visit | Number of visits per study participant | Anticipated start date for CRC Services | Anticipated end date for CRC Services | Funding source | Full study name | Primary Investigator's full name | PI's email address | PI's primary phone | Key personnel who will interact with study participants | Study Protocol | IRB Approval Letter | Stamp-approved consent/assent forms | Is your study is being conducted under an IND or IDE? | Investigator’s Brochure or device manual (for all investigational products) | Is this a clinical trial? | Is this study investigator-initiated? | Entry ID | Source URL | User | User IP |