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Importation of Medicinal Products into the European Union

by Rachel (Gatt Rutter) Percival, GMP/ GDP Compliance Principal Consultant & Qualified Person @PQE Group

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A focus on Batch Certification

The Importation of Medicinal Products into the European Union is complex and comes with several requirements ranging from licenses and authorizations to the Qualified Person, Batch Certification and Post Marketing activities.  

 
Importation Medicinal EU_site PQE

PQE Group can support all of these inter-related services and requirements, for both regulated and non-regulated markets, through our federated partner, Quintian Pharma, which is committed to providing services and support to the pharmaceutical industry, following all EU directives on new products.

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