Achieving a consistently high quality of preparations is always our top priority at bene-Arzneimittel. To this end, we strictly implement and adhere to the requirements of the EU GMP (Good Manufacturing Practice) guidelines and EN ISO 13485 in all areas.

Patient and product safety

Product safety and the resulting patient safety are achieved through transparent procedures and continuous monitoring and documentation of quality-relevant measures. Continuous improvement of processes further contributes to high quality.

Cutting-edge manufacturing and testing procedures

Manufacturing and testing are performed by qualified staff members only, following written specifications.
All starting materials are tested before use. The produced drugs are placed on the market only after Quality Control has tested them using suitable methods and the Qualified Person has released them after viewing all product-related documents. As a result, we achieve top product characteristics and very high, consistent quality.

Implementation of customer requirements

By continuously improving all processes, bene expertly and reliably implements individual customer requirements.
 

Certificates 

GMP-certificate (German)
Manufacturing authorisation bene-Arzneimittel GmbH (German)