Connect and Interact with Industry, Academia, and Regulatory Experts from Around the World - Fall DIA

Connect and Interact with Industry, Academia, and Regulatory Experts from Around the World. DIA’s educational portfolio addresses all of today’s hottest topics, including biosimilars, PDUFA, rare diseases & orphan products, medical devices and diagnostics, as well as the new research and analysis that’s occurring after a product has been approved and available in the marketplace. Plan Now for the Fall! DIA/FDA Biosimilars Conference: Guidances, Science, and BsUFA September 12-13 | Washington, DC DIA/FDLI Unwrapping FDA’s 2012 UFA Package: What’s Inside the Statute, What’s Next? September 20 | Washington, DC EDM and ERS/eCTD: The Content Continuum from Document Authoring through Submission Delivery October 8-11 | Baltimore, MD Register by September 17 to Save! Principles and Practical Approaches to Global Benefit-Risk Management October 9-10 | Silver Spring, MD Register by September 18 to Save! Global Labeling 2012: Impact on Risk Management & Other Global and Regional Initiatives October 11-12 | Silver Spring, MD Register by September 20 to Save! DIA/FDA Industry PDUFA V Conference October 18-19 | Arlington, VA US Conference on Rare Diseases & Orphan Products: Shaping the Future Now October 22-24 | Washington, DC Register by October 1 and Save! DIA/FDA: Revitalizing R&D Productivity in Drug Development October 23-24 | Bethesda, MD DIA’s Annual Canadian Meeting: Evolutions in Risk Thinking November 5-7 | Ottawa, ON Canada Register by October 19 and Save! FDA Information Day: Individual Case Safety Reports (ICSR) November 29-30 | Silver Spring, MD   Save the Date: DIA Combination Products Regulatory Workshop: Approval Pathways for Drug/Device Combinations and Companion Diagnostics November 7-8 | Washington, DC Data Monitoring Committees: Best Practices and Future Directions November 2012 | Washington, DC