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Trial Master File Reference Model Discussion Forum
Trial Master File Reference Model Discussion Forum

(a Community Group now part of CDISC)

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Trial Master File Reference Model Discussion Forum
Trial Master File Reference Model Discussion Forum

(a Community Group now part of CDISC)

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Topics Engaged In

Viewing 6 topics - 1 through 6 (of 6 total)
    • Topic
    • Voices
    • Posts
    • Last Post
    • Non-IP supply destruction documentation

      Started by: Stephanie Hayden in: Where do I file…. ?

    • 2
    • 2
    • 1 year, 10 months ago

      Meredith Lafond-Phesans

    • Auxiliary medicinal product

      Started by: Vanessa Tarraga in: Where do I file…. ?

    • 3
    • 3
    • 2 years, 7 months ago

      Rebecca Siegl

    • Institutional biosafety committee (IBC) Documents

      Started by: Kathie Clark in: Where do I file…. ?

    • 3
    • 4
    • 2 years, 10 months ago

      Meredith Lafond-Phesans

    • TMF RM_EU Clinical Trials Regulation 536/2014

      Started by: Maria Pedko in: Where do I file…. ?

    • 3
    • 4
    • 3 years, 3 months ago

      Karen Roy

    • EU CTR – Compliance with use of Biological samples

      Started by: Meredith Lafond-Phesans in: Where do I file…. ?

    • 3
    • 4
    • 3 years, 3 months ago

      Karen Roy

    • Local Lab Documentation – ISF only?

      Started by: Meredith Lafond-Phesans in: Where do I file…. ?

    • 2
    • 2
    • 4 years, 7 months ago

      Richard Golden

  •  

Viewing 6 topics - 1 through 6 (of 6 total)

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

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