Skip to content
NNIT at DIA RSIDM (Regulatory Submissions, Information, and Document Management Forum)

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

Event date 12 February 2024 – 14 February 2024

Location 5701 Marinelli Road, North Bethesda, MD 20852 , USA

Our team in the US with Toni Lakin-Ritter, Cathleen Hynoski, Christopher Lucas, and Nicholas Rattenni will be present at booth #211, ready to welcome and discuss the latest trends, innovations, and best practices in regulatory submissions, information, and document management. The key message and focus of our booth are RA and Veeva solutions.

Furthermore, Samuel Thompson and Kåre Hyttel have been chosen as speakers to a Virtual Pre-Conference Short Course on February 8 ''Mapping Common Regulatory Data Standards to FHIR''. They will discuss, from a regulatory perspective, the similarities and differences among multiple data standards that are targeted for use in FHIR for data exchange, including:

  • Identification of Medicinal Products (IDMP)
  • Chemistry, Manufacturing & Controls (CMC)
  • Structured Product Labeling (SPL)
  • Electronic Medicinal Product Information (ePI)

Journalists are welcome to stop by the NNIT booth.

Categories

Contacts

Tina Joanne Hindsbo

Tina Joanne Hindsbo

Press contact Head of Public & Media Relations +45 3077 9578
Sofie Mand Steffens

Sofie Mand Steffens

Press contact Senior Communications Consultant +45 3077 8337

Related content

Unlock the true power of eTMF after going live

Unlock the true power of eTMF after going live

Implementing an electronic Trial Master File (eTMF) system can revolutionize the way clinical trials are managed. However, as Michael Agard, Director of Clinical Consulting at NNIT, points out, the true value of eTMF lies in post-implementation management.