Already a DIA Member? Sign in. Not a member? Join.

Iniciar sesión

¿Ha olvidado su ID de usuario? or ¿Ha olvidado su contraseña?

Not a Member?

Create Account and Join

Bethesda North Marriott Hotel and Conference Center

08 feb 2027 10:00 a.m. - 10 feb 2027 12:45 p.m.

5701 Marinelli Road, North Bethesda, MD 20852

Regulatory Submissions, Information, and Data Management Forum

Don't miss the latest trends, innovations, and best practices in regulatory submissions, information, and document and data management (RSIDM)!

Early Bird Ends In

DAYS

HOURS

MINUTES

SECONDS

Perspectiva general

February 8-10: Forum

As regulatory operations continue to evolve, organizations are increasingly being challenged to move beyond document-centric processes toward more connected and data-enabled ways of working. Success today depends not only on the ability to prepare and deliver high-quality submissions, but also on how effectively organizations manage information, structure data, optimize processes, and align the people, systems, and technologies that support regulatory work.

At DIA’s Regulatory Submissions, Information, and Data Management (RSIDM) Forum, industry and regulatory stakeholders come together to examine the standards, requirements, technologies, and approaches shaping the current and future state of regulatory operations. While the RSIDM acronym remains unchanged and continues to reflect the Forum’s established identity, the inclusion of “Data” in the meeting name more accurately reflects the growing importance of data in regulatory submissions, information management, process improvement, and technology adoption.

Through four focused tracks, the Forum provides practical insights on how to build and sustain strong RSIDM foundations, optimize processes and procedures, adopt innovative technologies, and strengthen strategic leadership and organizational readiness. The Forum also offers opportunities for education, networking, and knowledge sharing for both business- and technology-focused professionals at all levels.

While we develop our 2027 agenda, please take a moment to review the 2026 final agenda

Featured

Want to learn more about Regulatory Submissions, Information, and Data Management Forum? You've come to the right site!

¿Quiénes deben asistir?

  • Forum Designed For

    • Clinical Data/Data Managers
    • Clinical Operations and Processes
    • Contract Research and Service Support Providers
    • Document and Records Management/Specialists
    • Emerging Pharmaceutical/Biotech/Device Professionals
    • Essential Document Process and Business System Owners
    • Informatics/Bioinformatics Professionals
    • Information Technology and Support Personnel
    • Medical, Technical, and Regulatory Writers
    • Outsourcing/Clinical Outsourcing
    • Quality Assurance/Quality Control and Compliance Professionals
    • Quality Management
    • Regulatory Affairs and Operations
    • Regulatory Informatics
    • Regulatory Information Management
    • Regulatory Standards Implementation Specialists and Associates
    • Strategic Planning and Operations
    • Submissions and Global Submissions Management/Project Management
    • TMF and eTMF Management
    • Vendor Relationship Managers

Digital Learning Catalog

DIA Learning: eLearning Soultions
Download

¿Tiene una cuenta?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.