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Whether we are referring to CSRs or to IPD, the personal information of trial participants needs to be de-identified prior to release. This article will describe the available methods for de-identifying clinical trial data, and the relative strengths and weaknesses of each.

CRO/Sponsor: Logical Sourcing: Key Steps Clinical Technology: eSource Record-Keeping Data Sharing: De-identifying Trial Data Also in this issue: R&D Focal Points in Europe Patient Centricity: The Clinical Investment PRO Plusses for Diabetes Research