Using the Facility

Please contact the core director to schedule an initial consultation regarding the correlative studies you are proposing for your clinical trial. A research plan will then be assembled by the director and submitted to the principal investigator for approval. A lead time of three to six months is generally required for protocol development.
Note: Equipment operation is restricted to qualified CICSL personnel.
Quality Control
Protocol development, instrumentation, reagent, and technical quality control in the CICSL will be guided by GLP principles of operation. To the extent possible, all CICSL equipment is compliant with 25 CFR part 11 guidelines.