Posted By
Peter Miko
17-Jul-2022 23:21
Found In
Egroup:
Regulatory Open Forum
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Dear Colleagues, after reading the 1st mail, my understanding is, that the concerned syringe containing the diluent of the medicine is part of the finished pharmaceutical product, therefore for the approval of the Marketing Authorisation of the medicine, the syringe in the EU needs to be either ...
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