As part of its advocacy program in Europe, ACRO submits regulatory comments to European officials. This comment letter, submitted by ACRO to EU>European Commission in 2016 about Summary of Clinical Trial Results for Laypersons can be found below.
As part of its advocacy program in Europe, ACRO submits regulatory comments to European officials. This comment letter, submitted by ACRO to EU>European Commission in 2016 about Summary of Clinical Trial Results for Laypersons can be found below.