NNIT at the DIA Regulatory Submissions, Information, and Document Management (RSIDM) Forum

The last few years have shed light on the importance of operational efficiency of the management of regulatory information to ensure quality regulatory submission to health authorities. The ability to perform at this level has allowed drug companies to bring therapeutics and vaccines to patients faster.

At DIA’s Regulatory Submissions, Information, and Document Management (RSIDM) Forum, you can meet industry and regulatory stakeholders working across the scope of regulatory information to examine current and evolving data standards and requirements and effective regulatory information management approaches to align related people, processes, and technology - including NNIT.

The NNIT team will be at exhibit booth #107. Journalists are welcome to stop by to learn how regulatory expertise, technology acumen, and practical understanding of document and data creation, management, and reuse, can help to reduce errors and increase efficiency within life sciences.

Three of NNIT’s advisors will also be presenting at the conference:

1. Michael Agard, Team Leader, Clinical Consulting US, will present “Analyzing TMF Finding Data to Drive Process Improvement.”
   Tuesday, Feb 14, 2023, at 11:15 AM – 12:30 PM: Session 6, Track 3: Advancing Inspection Readiness Through Data-Driven Planning and Continuous Process Improvement.
   
2. Katherine Novak, MS, Senior Advisory Consultant, Life Sciences will chair a discussion on "Is it Time to Streamline Your Processes with Structured Content Management?"
   Tuesday, Feb 14, 2023, at 2:00 PM –3:15 PM: Session 7, Track 2.
   
3. Sam Thompson, Managing Consultant, will present, “Is Your Data Ready for RIMS?”
   Wednesday, Feb 15, 2023, at 10:30 AM - 11:45 AM: Session 10 Track 1: Regulatory Informatics – Business.