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Follow on Google News | Only Regulatory Affairs CMC Event Back for Second YearInternational Guidelines, FDA Meeting Preparation Strategies Among New Discussion Topics
By: Q1 Productions 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/ About the Organizer Q1 Productions designs and develops webinars, training courses, conference programs and forums aimed at specifically targeted audiences throughout highly regulated industries in order to provide strategic learning and timely program content. Through a highly structured production process focused on research calls with end-users and key stakeholders in the industry, our team is able to understand the immediate business concerns of today's leading executives. Whether focusing on new or pending legislative and health policy issues or enhanced technologies or processes that will drive efficiency, our programs provide solutions to the urgent educational and information needs of our attendees. End
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