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Closing Humira Inquiry, Ombudsman Advises EMA On Future Trial Data Redaction

This article was originally published in SRA

Executive Summary

The European Ombudsman, Emily O'Reilly, has closed her inquiry into the European Medicines Agency's release of a number of redacted clinical trial study reports on AbbVie's MAb Humira (adalimumab), and has made a number of recommendations as to what the agency needs to do to ensure that the maximum amount of trial data is made publicly accessible in future1.




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