PHOENIX quality

The Department of Quality is in charge of continual improvement of the quality management system, as one of the aims of PHOENIX Farmacija quality policy.

Compliance of business operations with the GMP requirements for the wholesale of drugs and European GDP guidelines is continually monitored, and the results PHOENIX Farmacija achieves are always outstanding.

Quality management is carried out by monitoring implementation and continually improving internal standard operative procedures (SOPs). These procedures cover checking, receiving and handling products, distribution and transport, maintaining warehouses, educating employees, internal audits, receiving, storing and distributing products for clinical research, instructions for emergency situations, such as cold chamber malfunction, recalling products etc. Standard operative procedures are aligned with valid European GDP guidelines, the requirements of European GMP and national regulations.

Operations of both the consignment and other warehouses of PHOENIX Farmacija are regularly audited by our principals, receiving always the highest of grades.

Manufacturing licence and Good Manufacturing Practice

For the purpose of packaging PHOENIX Farmacija has cooperated with experts in the area of Good Manufacturing Practice and has reconstructed the 254 m2 of the warehouse in Velika Gorica Centre, in accordance with the requirements for secondary drug packaging, with a cold chamber for the packaging of thermally unstable products, the so-called cold chain.

The quality system and manufacturing facilities have met the criteria of the Agency for Medicinal Products and Medical Devices inspections, and PHOENIX Farmacija has been issued a manufacturing licence which enables the following:

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PHOENIX Farmacija meets the highest business standards.