QP Association forwards consolidated Comments to European Commission Draft Template for QP Declaration concerning GMP Compliance of IMPs
In February the European Commission issued a draft of the "Template for the qualified personís declaration concerning GMP compliance of investigational medicinal products manufactured in non-EU countries" and invited stakeholders to comment on this draft by 2 April.
The Association's IMP Working Group collected comments from its members and now forwarded the consolidated document to the Directorate-General for Health and Consumer Protection (DG SANCO.
You can find the consolidated comments of the group here.
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