More than a decade has passed since the U.S. medical device industry began to implement strategies to comply with the FDA quality system regulation. But for company leaders, the creation of appropriate quality systems that bridge the areas of research, development, and manufacturing remains an activity that is fraught with business and regulatory risk. In this
FREE Webcast, “Managing Risk at the R&D–Manufacturing Interface,” hosted by
MX magazine and sponsored by
Oracle, industry experts provide insights into the trends driving the development and implementation of advanced quality systems for life sciences companies. Presentations examine key processes for automating the transfer from R&D to manufacturing to improve business efficiency and support compliance integrity.
