Description
Worldwide expenditure on R&D by the pharmaceutical industry is continually increasing. Most of the financial investment in the production of a new drug is allocated to clinical trials.
Given the financial risk involved, it is crucially important that clinical trials be designed and set up efficiently to obtain adequate and accurate data in compliance with regulatory requirements.
This module aims to provide information on clinical trials data capture and management. This session describes the purpose of data capture and explores efficiencies in data management as part of the evolving regulatory landscape.
