QP Release
- Qualified Person
- QP Release
- EU Batch certification/ EU Batch -Release
Each and every batch of investigational or market-authorised medicinal products used in the EU, whether imported as bulk or as finished products, has to be certified and released by a Qualified Person.
Delivery to customers (patients) takes place only after our Qualified Person has certified every production batch has been produced and controlled in accordance with the relevant legal requirements and any other regulations relevant to the production, control and release of medicinal products.
This certification process, including the EU Batch Release, applies to medicinal products imported from outside the European Economic Area, as well as batches that undergo labelling and packaging procedures in house, and assures that the quality of all our shipments complies with the highest possible quality requirements.
