Stop by at Booth # 305 and join DDi at DIA RSIDM in Bethesda North Marriott Hotel, MD on 6-8 February 2017. DDi provides smarter technology for Regulatory areas with key focus on Automation utilizing AI/NLP. In addition, DDi has next generation tools like VISU (RIMS), MPDsmart, cmcXtract, smpXtract and LabOps (for Labeling).
Meet the team DDi at DIA’s Regulatory Submissions, Information, and Document Management Forum, which is one of the premier consortium for the discussion of emerging operational standards, best practices, and the processes for submission, creation, and maximum use of regulatory information. The forum explores information generated along the drug development continuum life cycle and alignment to ever evolving regulatory and electronic standards.
The RIM Business focused track provides the opportunity to interact and share experiences related to processes for obtaining and managing regulatory information and the organizational impact, as well as gain a greater understanding of key issues shaping the global regulatory environment. It also focuses on standards related to submission of regulatory information, the tools necessary to effectively manage the information, and associated implementation experiences and lessons learned.
