Outsourcing in the life sciences industry is an established business practice that saves time and money. Medical device post-approval studies differ in both subtle and considerable ways from that of drugs or biologics, including how to approach and conduct mandated post-marketing studies. Successful partners in this realm require a firm understanding not only of the regulations, but also how to nurture seamless, high-functioning project teams.
This conference provides insights into building successful CRO partnerships that focus on medical device manufacturer needs, including risk analyses, communication plans, safety considerations (adjudications and DSMBs), effective team building and setting milestones and metrics to track success.
Effective Strategies for Successful Medical Device-CRO Partnerships in Post-Approval Studies is being presented by Yvonne Albright and Barbara Vargas, Project Managers, with Covance Periapproval Services and airs on Thursday, April 16, 2009. For more details or to register, please visit our site at www.fxconferences.com
