Medical Supervision

CIRG guarantees medical supervision for each of its studies. 

Any medical question or issue raised by the sponsor, an investigator, CIRG personnel, etc is addressed by a medical oncologist within CIRG.  Serious adverse events are medically reviewed as soon as CIRG is notified.

The oncologists are involved in the writing and/or reviewing of all medical documents, which include the protocols, final study reports, abstracts and publications. 

CIRG offers its employees a formal monthly training program in clinical trials research, general oncology, breast cancer and its standard and experimental treatments, and translational research through tele- and videoconferencing.