Delfarma

We make sure the standards of Polish drug laws are 100% met before we release our products to wholesale distributors, pharmacies and hospitals. Using carefully protocolled procedures the products are collected and given a Polish-language information leaflet and the necessary labels. This work demands optimum attention to detail and alertness on the part of the employees. Intensive quality control processes prevent errors. Medicines are vulnerable products, that is why Delfarma pays careful attention to transport and storage. Temperature is a very important aspect. Many products need to be stored in temperature-controlled conditions. This places high demands on storage capacity and transport companies. Delfarma is approved as a company for parallel import of pharmaceuticals by the responsible authorities and holds a manufacturer and distribution license, which entitles us to repackaging and distribution of pharmaceuticals. Delfarma is also closely monitored by national and European institutions such as the European Medicines Agency. Delfarma works together with wholesalers in EU countries, of which all have a valid wholesaler license and a quality system in accordance with the most current Good Distribution Practice (GDP) guidelines. Our suppliers are regularly audited by their local authorities. Additionally, Delfarma has its own supplier qualification system, which sets high standards in operational processes as well as quality and which is continuously being enhanced by our team. Only products, which are performed in accordance with GMP and GDP standards, are released for shipment to our customers. Delfarma means the highest quality proven with ISO 9110:2008 certificate issued by TÜV SÜD. Processes in our company fully conform to the Good Distribution Practice (GDP) and Good Manufacturing Practice (GMP).