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EU harmonisation of Qualified Person's Declarations for clinical trials

03 December 2013

The European Commission has published a template for the Qualified Person’s Declaration Concerning GMP (Good Manufacturing Procedure) Compliance of the Investigational Medicinal Products. 

The aim of the new QP declaration is to harmonise the documentation in the EU.

We encourage companies and researchers to use this declaration in future.

You can find the declaration on the website of the EU Commission