About the Conference
Now in its seventh year, this unique forum continues the dialogue on issues including FDA guidance development and regulatory science initiatives including PDUFA V initiatives. The dialogue will focus on statistical opportunities and challenges associated with data standards and innovative approaches to the design, monitoring, analysis and reporting of clinical trials and assessments of safety and effectiveness in the pre- and post-market settings.
You may register online or download a registration form. For registration questions, please contact CustomerService@DIAHome.org or at +1.888.257.6457.