EUCROF responded to the EMA’s consultation on the 'Draft proposal for an addendum, on transparency, to the “Functional specifications for the EU portal and EU database to be audited' (EMA/42176/2014). On behalf of its members, EUCROF actively participates in the ongoing discussions and stakeholder meetings in relation to the implementation of the EU Clinical Trials Regulation. We would welcome any feedback or comments. [Eucrof comments EMA consultation on draft proposal for addendum on transparency]
