10 February 2020

The DIA Regulatory Submissions, Information, and Document Management (RSIDM) Forum provides attendees with the information they need to meet all the challenges that come with managing regulatory information, including processes, tools and examination of results. 

DIA RSIDM will present four tracks this year, including RIM Business, RIM Technology, Electronic Document Management (EDM), and Electronic Regulatory Submissions (ERS). These tracks will be filled with speakers and experts from prominent faces in the Life Sciences industry, with representatives from organizations such as the FDA, Health Canada, and other major organizations.  

At the DIA RSIDM Forum, attendees will have the opportunity to network, exchange ideas, and become educated on a variety of topics.

The Amplexor Life Sciences team will be on-hand to answer your most pressing questions about regulatory information management. Also look for us to be leading one of the sessions! 


Throughout the DIA RSIDM forum, Amplexor's Life Sciences team will be available at Booth #104 to discuss your RIM and submission management challenges, offering insights and strategies to help you achieve your business objectives. In addition, Abbott's Director of Regulatory Affairs John Bates will be available to discuss the most recent industry case study, "Delivering On a New Document Management and RIM Platform – Vendor Selection to Deployment."