Clinical trial data can offer a treasure trove of insight – but first it needs to be unlocked.

The number of clinical trial data sets available for secondary analysis has been growing steadily over the last year. While encouraging, there is a need to also ensure that this data is properly de-identified.

The webinar Double-Blind will set expectations about what is needed in a de-identification solution for clinical trial data, and offer a pragmatic look at emerging standards in this area.

Key Learning Objectives:

  • Review the standards and regulations in place;
  • Understand the risks and mitigate them; and,
  • Learn what de-identification is and isn’t–then how to apply it to clinical trial data.


Khaled El Emam, CEO
Luk Arbuckle, Director of Analytics

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