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February 10 - February 12

Document transformation and Belgian chocolate

DIA RSIDM 2020 – Regulatory Submissions, Information and Document Management Forum

A brief conversation and your Belgian chocolate is waiting for you at the DIA RSIDM conference.

Click here to schedule a moment to pick up your chocolate.


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.

DIA RSIDM Official 2020

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.