​​​Join us at booth #101 at the DIA Regulatory Submissions, Information, and Document Management Forum. DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum provides the elements needed to meet the challenges of optimizing the efficient use of regulatory information: the RIM principles, effective processes and tools, benefits to data applications across the product lifecycle, and examination of real-life results.

DIA will present four tracks and daily health authority plenary sessions to provide a comprehensive view of content and regulatory information management and submissions:

  • ​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 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 explores the submission process, regulatory requirements and new developments, best practices in regulatory submissions and industry adoption techniques.
  • 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.

​The Forum provides multiple opportunities for networking, knowledge sharing, and education for both business- and technology-focused attendees. Come and meet our team and learn more about our solutions using the innovative InteliNotion  Intelligent Content and Information Management platform.

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