FDA PRO Guidance and ePRO patient reported outcomes solutions with patient eDiaries

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PHT regularly interviews and solicits feedback from principal investigators and study coordinators who have experience using our LogPad System and SitePad Tablet in more than 360 clinical trials around the world … Here's some of what we've learned so far.

Steve Raymond, Ph.D. Founder, Chief Scientific and Quality Officer

Read more on what people are saying about PHT.

European Webinar: A Day in the Life of a Data Point

European Webinar: A Day in the Life of a Data Point

Clinical research sponsors in Europe are increasingly relying on technologies to reduce their clinical data management burden and accelerate their clinical trials. As they choose the most suitable systems for their environment, they also face questions about best approaches for data-sharing across these systems.

Listen to this webinar recording to examine the life of a data point in an eClinical environment and review best practices for leveraging clinical technologies. Speakers Valdo Arnera, General Manager at PHT Corp, and Richard Young, Director of Regional Sales, EMEA, at Medidata, will highlight:

  • The life of a data point, from protocol generation to data capture — including electronic patient reported outcome (ePRO) systems and electronic data capture (EDC) systems — and comprehensive data management and analysis;
  • Best practices for using ePRO and EDC in European trials, including insights on the recently finalized FDA PRO Guidance;
  • Two approaches for using ePRO systems alongside EDC systems, including an examination of data traceability and ownership; and
  • The data management advantages offered by an integrated ePRO-EDC approach.

Download webinar here.

Clinical and data professionals who listened to this webinar also downloaded 'Why Paper Diaries Should Be Banned' by Valdo Arnera, and the Insights Issue entitled 'PHT Auditing Quality & Compliance".

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