Halloran's Kathi Shah explains how to create a compliant, lock-tight clinical trial site budget.
By Kathi Shah, MS, MBA
Creating a clinical trial site budget sounds simple right? A Sponsor contracts with an investigative site to conduct a clinical trial per the protocol. The Investigative site is compensated by the Sponsor to conduct the services outlined in the protocol. The relationship between the Sponsor and Investigative site is heavily weighted on the budget developed to compensate sites for their efforts to conduct the study.
from MassDevice - FDA and Medical device business news and jobs for the medical device industry http://ift.tt/1LM7uxb
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