Regulatory Submissions, Information, and Document Management Forum

Bethesda, MD

February 10 - February 12, 2020

Bethesda, MD |

DIA’s Regulatory Submissions, Information, and Document Management 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. All tracks are supported with daily plenary sessions providing regulatory intelligence updates by health authority representatives from FDA, Health Canada, and other regions of interest.

Accepted Abstract #: 86393

Abstract Title: The vision and reality of AI and Automation to accelerate Regulatory Information and Knowledge Management. (RiaKM)
Presenter: Matt Neal, Senior Director, Product Management, Regulatory & Clinical Solutions

 

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