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 systems. The Forum presents four tracks: Regulatory Informatics Business, Regulatory Informatics Technology, 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.
Join IQVIA in the sessions and in our exhibit to discover how to streamline your regulatory compliance systems and processes with end-to-end regulatory technologies, advisory and tech-enabled services. Free your team from labor-intensive tasks and maintenance to focus more on delivering valuable products to market.