What is happening at Regulatory Submissions, Information, and Document Management Forum

• Four educational tracks: RIM Business, RIM Technology, Electronic Regulatory Submissions (ERS), and Electronic Document Management (EDM)
• One full day Preconference Primer: Regulatory Content and Submissions - Content from Authoring to Archive *Additional fee required
• Two half day Preconference Short Courses *Additional fee required
• Exhibit Hall with 40+ exhibiting companies
• Solution Showcase Theater in the Exhibit Hall highlighting innovations from Solution Providers
• DIA Mobile App - receive all need to know information, build your agenda, and network with attendees

Preconference Primer and Short Courses

February 9 | 10:00AM-5:00PM

• Regulatory Content and Submission Primer: Content from Authoring to Archive

February 10 | 8:30AM-12:00PM

• 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

RIM Business Track

The RIM Business track addresses processes for obtaining and managing regulatory information, organizational impact, and key issues shaping the global regulatory and business environments

RIM Technology Track

The RIM Technology track focuses on standards related to submission of regulatory information, tools to effectively manage the information, implementation experiences and results, and implications for refinement

Electronic Regulatory Submissions (ERS) Track

The Electronic Regulatory Submissions (ERS) track explores the submission process, regulatory requirements and new developments, best practices in regulatory submissions and industry adoption techniques

Electronic Document Management (EDM) Track

The Electronic Document Management (EDM) track examines the processes, systems, and best practices for content management across the product lifecycle, including alignment with the RIM system for optimal use of regulatory information