Study Set-Up
Main Content
Lab
Definition
- A lab may be utilized for the processing and shipment of clinical research study participant specimens.
Policies/guidelines
- The collection of specimens should only be performed by trained clinical research coordinators or staff members.
- Personnel collecting participant samples should verify that full informed consent and authorization has been obtained from the participant or their legal authorized representatives prior to sample collection.
- Specimens should be collected according to the protocol of the clinical trial, while also adhering to the appropriate safeguards from Occupational Health and Safety (OSHA) guidelines.
- Collection and processing of specimens must take place in a regulated clinical space, BSL-2 research lab, Clinical Research Support Program (CRSP) space, or the BioBank.
- IBC approval may be required for specimen collection, processing, and shipping. See the IRB/ Ancillary Committee Review section for more information on the specific requirements for IBC approval regarding specimens.
Resources
- Clinical Research and Trials Unit (CRTU)
- Services: Research sample processing, storage, and shipment.
- Contact: Email Cathy Hudgins, Research Nurse Manager, or call (601) 815-9276.
- UMMC Biobank
- Services: Biospecimen management including tissue procurement, blood processing, banking collections, shipping, and dry ice.
- Contact: (601) 815-3174
- Clinical Research Support Program (CRSP)
- Services: Clinical research coordinator services including sample collection, processing, and shipping.
- Contact: Kimberlee McGuire, Manager Research Operations, (601) 815-9955.
Training
- Lab draws and processing - PDF