One of the main objectives within the CDISC technical roadmap released in 2008 was to conduct pilots to gain a better understanding of the needs of regulators and industry. Based on this objective, a number of pilot projects have either been completed or are ongoing. Chris Decker, Life Sciences Director at d-Wise Technologies, will chair this session that will provide an overview of three ongoing pilots involving collaboration between CDISC and the FDA with the goal of obtaining efficiencies from the use of data standards.
