6-Hour Virtual Seminar on eCTD Submissions of IND-NDA to the US FDA, EU and Canada

If you are unable to see the message below, [click here to view](. [Logo]( 6-Hour Virtual Seminar [6-Hour Virtual Seminar on eCTD Submissions of IND-NDA to the US FDA, EU and Canada]( [REGISTER NOW]( This webinar will provide you with information to ensure that you are ready for implementing the mandated requirements of the CTD/eCTD. Date: Thursday, November 21, 2019 Time: 08:00 AM PST | 11:00 AM EST Duration: 6 Hours Instructor: Peggy Berry Overview: The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. [Read more..](. Who Will Benefit: - Regulatory Affairs - Quality Assurance - Pharmacovigilance - Project Management - Regulatory Operations - Anyone responsible for providing content for the CTD About Speaker: Peggy Berry President & CEO, Synergy Consulting Peggy J. Berry MBA, RAC, is the President & CEO at Synergy Consulting where she provides consulting services to companies in all aspects of drug development. She also provides group and one-on-one training in drug development, regulatory affairs and project management topics. [Read More]( GlobalCompliancePanel 39658 Mission Boulevard, Fremont, CA 94539, USA. Toll Free: +1-800-447-9407 Fax: 302 288 6884 [www.globalcompliancepanel.com]( | [Unsubscribe]( Copyright © 2019 GlobalCompliancePanel. All rights reserved.