Manufacture and quality

As a manufacturer of medicinal products and medical devices, our responsibility stakes are particularly high. In order to face these responsibilities, we have implemented a comprehensive quality assurance system. Furthermore, as a manufacturer of medical devices, we have also been certified according to DIN EN ISO 13485: 2003.

Every year, Pohl-Boskamp despatches around 16.5 million packages. Our quality control system must therefore be elaborate and technically sophisticated. With this in mind, we have developed many innovative - often automated - procedures.

Pohl-Boskamp, along with its employees, is constantly audited by governmental institutions. Due to our activities on the US market, we are also subject to monitoring by the FDA (Food and Drug Administration). Such bodies regularly confirm that - with regard to manufacturing and quality control - Pohl-Boskamp operates in full compliance with internationally valid requirements of Good Manufacturing Practice.

We offer a wide array of different pharmaceutical forms, as we adapt them to the needs of the patient. To enable us to manufacture and package such a wide product mix, Pohl-Boskamp has uniquely developed an extensive range of manufacturing skills, which allow flexibility and efficiency in investment projects.