Module 12 2019
How is a TMF Organised
Zone
Section
Artifacts
1.
Trial Management
Each Section is further defined into artifacts
Each zone contains specific sections that are standard by the industry
2.
Central Trial Documents
These documents can be defined specific to the company processes
3.
Regulatory
Generalized topics
4.
IRB/IEC and other Approvals
5.
Site Management
Documents can be blinded or unblinded
6.
IP and Trial Supplies
7.
Safety Reporting
Core TMF documents are required per industry standard
8.
Centralized Testing
Recommended TMF documents are suggested per the industry
9.
Third Parties
10.
Data Management
11.
Statistics
DIA TMF reference model v.3
The Organisation for Professionals in Regulatory Affairs
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