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Making eSource Work: Beyond the Hype

White Paper

Patient data drives clinical research, and the industry is transforming to improve the way data is obtained, which will ultimately allow patient-saving therapies and treatments to be brought to the market earlier to improve the lives of ourselves, our families and our friends.

One such transformation is the use of electronic source data, or eSource. However, eSource has not been adopted as quickly as expected based on the perceived and real benefits of moving toward electronic data collection. The benefits of higher quality data, less monitoring and better efficiencies are well understood and valued, but these have not yet inspired wide-scale adoption. For sites, it can mean operating differently from the norm, with potentially an initial layer of complexity before things become simpler.

Download our white paper to learn more about:

  • Benefits of eSource
  • Reasons for reluctance to implement eSource
  • Regulatory guidance regarding electronic source data
  • Considerations for implementing eSource
  • Getting started with eSource
  • SCDM eSource best practices


Leader in Clinical Trial
Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

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