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Regulatory Submissions, Information, and Document Management Forum

Don’t miss the latest conversations in RIM, EDM, and ERS! Join your industry colleagues and regulatory thought leaders and register for the Regulatory Submissions, Information, and Document Management Forum.

Resources

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Preconference Short Courses

Regulatory Content and Submission Primer: Content from Authoring to Archive

Short Course 1: Data at the Heart of Life Science Professionals: Instant Informed Decision Making

Short Course 2: Preparing and Submitting Standardized Study Data to FDA

Additional Information

Regulatory Affairs and Submissions Resource Kit

On Demand Content Preview Webinar

Status Update on the Implementation of IDMP