Protocol implementation and research sample acquisition:
- Before submitting clinical protocols to the CT-SRC and IRB, the investigator must first discuss the protocol with the Pharmacokinetics Shared Resource.
- After consultation with the protocol principal investigator (PI), a Request for Services form is sent to the PI; upon return of the form, protocol implementation is instituted, so that pharmacy, laboratory, and nursing staff are ready by the time the protocol is approved and opened.
Analytical assay implementation and ongoing quality control, biomedical modeling, study design and optimal sampling:
- The investigator contacts Drs. Baker, Crews or Panetta, or contact is made through regular Cancer Center Program meetings.
- Projects are reviewed by the PK Shared Resource Advisory Group for approval and prioritization.