The new IDMP standard is compelling life sciences organizations to rethink their RIM strategy, aiming to improve data quality and global collaboration. In fact, 86% are embarking on transformational change, according to a recent report. But with such a holistic change, how does one get started?
In Pharmaceutical Executive, Gordon Topping, senior director, submission portfolio and regulatory knowledge management, shares how UCB got an early start on IDMP preparations with a comprehensive strategy around data and modernizing their RIM capabilities. Read their six core objectives, and how you can get started.