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:
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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