International Guidelines, FDA Meeting Preparation Strategies Among New Discussion Topics
(Chicago) – For the second year in a row, regulatory affairs CMC professionals will have the opportunity to discuss the most top-of-mind challenges and latest guidelines they face today. Q1 Productions will host the 2nd Annual Global Regulatory Affairs CMC Conference October 13-14, 2016 in Philadelphia, Pennsylvania.
This one-of-a-kind event will provide regulatory affairs CMC professionals with in-depth discussions on a variety of topics, such as post approval changes on product supply chains, international regulatory guidelines, and CMC and QbD implementation outcomes. More than two dozen of the most influential and successful industry leaders will be on hand to lead sessions, case studies, and panel discussions, including Grace Rabano of Pfizer, Elsie DiBella of Shire, and Kathleen Sniff of Amgen.
The 2nd Annual Global Regulatory Affairs CMC Conference is the only meeting specifically geared toward regulatory affairs CMC professionals. This high-level conference provides a chance for attendees to network with peers, engage in in-depth Q&A, and share ideas on best practices and strategies.
For more information on the 2nd Annual Global Regulatory Affairs CMC Conference, please visit www.q1productions.com/regulatorycmc or email firstname.lastname@example.org. You can also follow the conference on Twitter @Q1Productions, @Q1CMC.