DIA RSIDM 2020 – Regulatory Submissions, Information and Document Management Forum
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About DIA RSIDM 2020
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.
DocShifter provides document conversion solutions to pharmaceuticals and life sciences: compliant submission ready PDF conversion, automating correspondence tracking, PDF/A conversion for digital archiving, legacy document transformation and automating the creation of standard templated forms.