At DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum, attendees 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. 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. 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 Regulatory Team will be at booth 204 and Sadia Ahmed will be presenting on Tuesday, February 14, 11:15AM - 12:30PM ET, in White Flint (Lower Level), where she will be presenting, "Journey to eCTD 4.0 standard: Simplifying the review of regulation."
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