Under European Union (EU) law, the Qualified Person (QP) is responsible for certifying that each batch of a medicinal product meets all required provisions when released from a manufacturing facility within the EU, or imported into the EU.
But a QP doesn’t just need expertise in manufacturing practice. They also need to understand the factors that can affect the safety of medicines and supply chains.
Here at Symbiosis, we have produced a quick infographic that outlays the roles and responsibilities of a Qualified Person, which you can download below.
Additionally, for further information on our Qualified Person release services, please visit our corresponding service page on the website or download our technical note on An Overview of the Qualified Persons’ (QP) Role in the Release of Batches of Biological Medicinal Products.
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