The more robustly and transparently the medical procedures are defined and documented, the more streamlined it gets during the study conduct and close-out phases. Further, the ground rules that structure the safety standards of the study and the integrity of the patient data collected are laid out during this phase. Mohamed El Malt, Chief Medical Consultant at Europital. & Vijayanand Rajendran, Clinical Research Physician at Europital, discusses in details the responsibilities and activities of a clinical research physician, the study MM, during the study setup phase – starting from clinical trial application till the recruitment of the first patient.
https://www.jforcs.com/7/wp-content/uploads/2016/07/Medical-Management.pdf