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Webinar
The Electronic Trial Master File: So Much More than Just
a Secure Document Repository
September 17 | 1:00-2:30 PM ET
Brought to you by DIA in cooperation with NextDocs
Implementing an electronic Trial Master File (eTMF) is becoming a standard business model for the clinical industry. The benefits of moving to an eTMF have been well documented, e.g. increased TMF quality, efficiency, and access to all stakeholders. However, there are additional benefits when considering the move to an eTMF, such asthe benefits gained from leveraging the data within the eTMF.
This FREE webinar will demonstrate how to leverage data to maximize the potential of an eTMF. Presenters will include Sharon Ames, Enterprise Program Director at NextDocs Corporation, and Gabor Fari, Director of Life Sciences Solutions at Microsoft Corporation.
September 17 | 1:00-2:30 PM ET
Brought to you by DIA in cooperation with NextDocs
Implementing an electronic Trial Master File (eTMF) is becoming a standard business model for the clinical industry. The benefits of moving to an eTMF have been well documented, e.g. increased TMF quality, efficiency, and access to all stakeholders. However, there are additional benefits when considering the move to an eTMF, such asthe benefits gained from leveraging the data within the eTMF.
This FREE webinar will demonstrate how to leverage data to maximize the potential of an eTMF. Presenters will include Sharon Ames, Enterprise Program Director at NextDocs Corporation, and Gabor Fari, Director of Life Sciences Solutions at Microsoft Corporation.
Featured topics:
- Using eTMF Data to Define and Measure Key Performance
Indicators and Operational Metrics
- Search vs. Findability – Obtaining Quick and Thorough
Query Results
- Using Interoperability and Standards for Streamlining
the Clinical Trial Process
- Ensuring the Availability of Data through Recommended
and Mandatory Metadata
Who Should Attend? Professionals involved in:
- Coordinating and Managing Clinical Trial Operations for
Drug Development in Sponsor or CRO Organizations
- Optimizing Clinical Trial Business Processes
- Administering and Reconciling TMF Records
- Overseeing Regulatory Compliance and Audit Readiness
for Clinical Trials
- Maintaining IT Infrastructure for Clinical Trials
