The optimal interaction between logistics, production planning and technology enables smooth, EU-GMP and EN ISO 13485 compliant manufacturing of liquid medicinal products and medical devices of the highest quality.
All manufacturing processes are subject to quality control and monitored by quality assurance systems. This is supported by regularly maintained and technically optimised infrastructure plus a well-established and continuously developed quality management system based on current EU-GMP and ISO standards.

We are happy to share our production know-how as a contract manufacturer, and we place the greatest importance on the fast, efficient and reliable processing of orders.


DI Dr. Bernhard Wittmann, b.wittmann et    Tel: +43-(0)1-330 0671-0
Mag. Dr. Michaela Freiler, m.freiler et    Tel: +43-(0)1-330 0671-61