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For more information, see: The Coordination Group for Mutual Recognition and Decentralised Procedures - Human (CMDh) and Coordination Group for Mutual Recognition and Decentralised Procedures - Veterinary (CMDv) have published information for marketing authorisation holders of nationally authorised products.A key condition for this exemption is that all necessary steps have been taken to prepare the transfer of the quality control testing site to the EU27/EEA.Marketing authorisation holders requesting the exemption must confirm and set out their precise timetable for transfering the quality control testing site.For procedural or regulatory queries related to type I variations for human medicines, contact [email protected] [email protected] human and veterinary initial marketing authorisation applications, EMA holds all pre-submission meetings requested as of 1 October 2018 remotely, either via teleconference or virtual meeting.