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

November 28, 2023 at 10:53 pm #5127
Debra WellsDebra Wells
Participant

Thanks, Eldin. Your opinion was in line with mine as well.

As an FYI, we are learning that this has been requested during inspections by FDA already, to some of the larger pharma.

Thanks again.

Post navigation
Next Reply →

Recent Discussion Topics

  • TMF DIA RM 3.2.1
    1 month ago
  • Date format in naming convention
    2 months ago
  • TMF – ISF mapping database
    4 months, 2 weeks ago

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