![]() Need approval in order to attend? Download and fill out our Justification Letter to demonstrate to your supervisor why this is a must-attend event. Preview all session descriptions, speakers, and more all in one place! I highly recommend this event!” - Regina Lynn Preciado, Content Rules, Inc. “Experts from all over the world generously shared their experiences, their lessons learned, and their recommendations for what we can do now and into the future. Can't recommend the event highly enough.” - Paul Ireland – DocShifter Unique opportunity to discuss solutions and industry topics with others in the industry. ![]() “Extremely useful event for any regulatory professional, or vendor providing solutions in the space. This Forum provides multiple opportunities for networking, knowledge sharing, and education for both business and technology-focused attendees. Cross-track sessions provide the opportunity to discuss key connection points across major components of regulatory information, and plenary sessions featuring regulatory intelligence updates by FDA and other regulatory authorities are offered each day. The Forum presents four tracks: Regulatory Informatics Business, Regulatory Informatics Technology, Trial Master File (TMF) Inspection Readiness and Electronic Document Management, and Electronic Regulatory Submissions. At DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum, we will hear from industry and regulatory stakeholders working across the scope of regulatory information to examine current and evolving data standards and requirements and effective regulatory information management approaches to align related people, processes, and technology. We have seen how the ability to perform at this level has allowed drug companies to bring therapeutics and vaccines to patients faster. Facebook gives people the power to share. Join Facebook to connect with Joel Agena and others you may know. ![]() The last few years have shed light on the importance of operational efficiency of the management of regulatory information to ensure quality regulatory submission to health authorities. View the profiles of people named Joel Agena. Time to Register! Keynote Announced! Ulo Palm, MD, PhD, MBA Chief Medical Officer Vaxxinity! By clicking SUBSCRIBE, you are agreeing to our Privacy Policy. ![]()
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