LOGOSYS' Integrated Quality Management guarantees that all storage, picking, transport and manufacturing processes are carried out in accordance with the GMP Directive, EN ISO 9001:2000, Section 13 of the German Drug Law (Arzneimittelgesetz), the German Ordinance on the Production of Pharmaceuticals and Active Substances (Arzneimittel- und Wirkstoffherstellungsverordnung), and the German regulation on wholesale distribution of medicinal products (Betriebsverordnung für Arzneimittelgroßhandelsbetriebe).

SOPs and COPs

All the relevant business processes, procedures and workflows are set down in the LOGOSYS Standard Operation Procedures (SOPs). We also document customer-oriented processes (COPs) in equal detail. We conduct our own regular inspections ensuring that the required procedures and workflows are understood by all LOGOSYS employees and consistently implemented in practice.

Spatial planning and facility management in conformity with GMP

The storage and production of medicines have to meet strict building planning and equipment requirements in order to conform to GMP: clearly separated zones for incoming and outgoing goods, storage, picking and manufacture, cleaning, access control, pest control and temperature mapping, to name but a few. Our experienced and skilled staff in purchasing and facility management ensure that all the relevant regulations are certain to be put into practice - to be safe.

Thorough training