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The Electronic Trial Master File: So Much More than Just a Secure Document Repository

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This Solution Provider Webinar is brought to you by DIA in cooperation with NextDocs. Registration for Solution Provider Webinars are FREE! Sign up by clicking on the Register Online button.

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…the 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.

Continuing Education credit is not available for the event.

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

Learning Objectives 

At the conclusion of this webinar, participants should be able to:

  • Understand common Key Performance Indicators and metrics and how they can be obtained from the eTMF
  • How to perform quick and effective search results from TMF content
  • Understand benefits of integration of eTMF with other clinical systems
  • Identify the metadata to be collected to achieve your business goals

Special Offers 

Registration for a Solution Provider Webinars is FREE! Sign up by clicking on the Register Online button.

Contact Information 

Registration Questions
Toll Free 1.888.257.6457
Phone +1.215.6100
Fax +1.215.442.6199
Monday-Friday 8:30AM - 8:00PM ET

Technical Requirements 

Click here for minimum system requirements.


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Day 1 Tuesday, Sep 17, 2013

  • 1:00PM - 11:59PM

    The Electronic Trial Master File: So Much More than Just a Secure Document Repository


    • The Electronic Trial Master File - Ames/Fari
      Sharon Ames
      Enterprise Program Director
      NextDocs, United States
    • Gabor Fari, MBA, MSc
      Director, Business Development and Strategy, Health and Life Sciences
      Microsoft, United States

Registration Fees 

Other Fees

Register Online

Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

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