EMA PleaseReview – for faster, controlled, collaborative document redaction of Clinical Data

The European Medicines Agency (EMA) Transparency Policy 70 requires that documentation must be redacted to remove Personal Private Data (PPD), Personally Identifiable Data (PID) and, optionally, Commercially Confidential Information (CCI). The submitting company must agree redactions (and provide a justification for each CCI redaction) to the EMA before providing finalized redacted documents for publication

This Data Sheet looks at how Ideagen PleaseReview helps simplify and streamline the redaction review process, allowing multiple people to co-author, review, and redact documents simultaneously.

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