The applicant should complete the XML delivery file and upload by the EMA Gateway.
Any submission that doesn´t comply may lead to delays in processing.
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Brexit updates for human use medicinal products approved via MRP/DCP
December 21, 2020
As Brexit is quickly coming closer, the CMDh has published an updated version of the Practical guidance for procedures related to Brexit for medicinal products for human use approved via MRP/DCP in December 2020.
