Webinars, White Papers and Seminars
Upcoming Live Webinars:
Reauthorization of MDUFA: Will you be affected?
Aptiv Solutions, in collaboration with CHI-California Healthcare Institute and Merrill DataSite®, invite you to attend a complimentary webinar presented by Ron Warren, Principal Consultant, who will review the Agency-industry negotiated agreement. You will learn about the important regulatory reform provisions added by Congress and what it all means for the medical technology industry.
When: September 25, 2012, 1:00 PM EDT / 10:00 AM PDT
Learn more and reserve your space today at http://www.elsevierbi.com/mkt/webinars/SP/AC092512Reg_CHIiframe.html#register
Featured On-Demand Webinars:
Adaptive Clinical Trials for Outsourcing Managers
This one-hour program will provide outsourcing managers and procurement professionals with a clear understanding of the importance of adaptive design trials for both patients and industry. You will learn how adaptive design trials can improve R&D efficiency and productivity, with a focus on specific procurement issues.
Reauthorization of the Prescription Drug User Fee Act (PDUFA): How Will You Be Affected?
by Amy Kneifel, Director, Regulatory Affairs, Aptiv Solutions
Post Market Risk Control for Medical Devices
by Judith Andrews, PhD, Director of Quality Compliance Services, Aptiv Solutions
Implementation of Adaptive Clinical Trials
as presented at the 2012 DIA Annual Meeting by:
Vladimir Dragalin, PhD, Senior Vice President, Clinical Trial Innovation Strategies, Aptiv Solutions
Mary Riggs, Senior Vice President, Global Operational Excellence
Jim Box, MS, MBA, Senior Director, Data Management, Aptiv Solutions
Aptiv Solutions talks about Adaptive Trials at the recent US DIA Annual Meeting
Hear Patrick K. Donnelly, Chairman & CEO of Aptiv Solutions speak about the benefits of using adaptive designs for clinical trials and best practices for implementing adaptive clinical trials.
To view our latest whitepapers and seminars, use the right navigation menu.
