Skip to content
Trial Master File Reference Model Discussion Forum
Trial Master File Reference Model Discussion Forum

(a Community Group now part of CDISC)

  • Home
  • Forums
  • Login
  • Subscribe
Trial Master File Reference Model Discussion Forum
Trial Master File Reference Model Discussion Forum

(a Community Group now part of CDISC)

  • Home
  • Forums
  • Login
  • Subscribe

Home › Forums › Where do I file…. ? › FDA mandatory Diversity Plan › Reply To: FDA mandatory Diversity Plan

January 26, 2024 at 1:38 pm #5134
Donna Dorozinsky
Participant

Hi Debra and Eldin, I would agree. I think filing this with the Trial Mangement Plan makes sense. If you system allows you to file to multiple studies at one time, but might be a good option.
Kind regards,
Donna

Post navigation
Next Reply →

Recent Discussion Topics

  • Questions related to TMF RM artifacts
    1 month, 3 weeks ago
  • eConsent validation documents
    3 months, 2 weeks ago
  • 10.02.05 Data Capture – Final Subject Data
    3 months, 3 weeks ago

Copyright © 2025 Trial Master File Reference Model Discussion Forum | Powered by Astra WordPress Theme