The conformity of our processes with the demands imposed by the German Regulation about the application of good manufacturing practice at the production of medicinal products and active ingredients and for the application of good expert practice at the production of products of human origin (AMWHV) has been certified within the framework of an audit by the Hamburg authority for social affairs, family, health and consumer protection.
The Pharma Product Group has laid down its procedures in its own GMP Manual; it works in accordance with own SOPs and has elaborated corresponding QM plans. The Pharma Product Group has its own independent quality assurance unit. These pharmaceutical procedures are integrated into the quality management system in accordance with DIN EN ISO 9001:2008, which is binding for the entire Lehmann&Voss&Co. KG.