Mar 1, 2021 · Real-World Studies Document Index Provides a proposed Document Index for use on real-world studies, based on the TMF Reference Model for clinical trials (v1.0 Approved 29 …

The Trial Master File Reference Model (TMF RM) User Guide is a simple to use resource for introducing the TMF RM, understanding its structure, and how to use it.

Jun 5, 2004 · The TMF Reference Model Steering Committee today announces that version 3.2.0 of the Trial Master File Reference Model is now available to download free of charge. The …

The TMF Reference Model initiative was formerly a sub-group of the Document and Records Management Community of the Drug Information Association (DIA). Since June 2022, it has …

Posts must be restricted to conversations about TMF Management and the Reference Model Project ONLY. Avoid asking questions that relate only to a specific commercial system.

The Trial Master File Reference Model (TMF RM) User Guide is a simple to use resource for introducing the TMF RM, understanding its structure, and how to use it.

TMF Reference Model User Guide – Provides step-by-step process for mapping your organization’s TMF to the TMF RM An improved presentation of the model will also be …

What is the procedure for filing essential documents and how will access to the TMF be granted to those who need it? These are just some of the questions that we hope can be answered by …

The result is a listing of core and recommended artifacts relevant to real world studies (that are not clinical trials) while remaining as consistent as possible with the TMF-RM format and …

The sponsor and the investigator shall keep a clinical trial master file. The clinical trial master file shall at all times contain the essential documents relating to that clinical trial which allow …