Media centre

Laboratory services and quality control
We provide analytical services of the highest level for active ingredients, excipients, medicinal products and drug-related products.
Have a look: In our video you get an overview of our laboratory services and quality control.

Drug Development
We show you the development, production and analytical testing of solid, semi-solid and liquid dosage forms. Have a look: In our video you get an overview of our services in drug development.

Tableting with high potent active ingredients
We show you the manufacturing of tablets with high potent active ingredients. In our clean rooms, solid oral dosage forms are being developed and small scale as well as clinical trial batches produced under GMP conditions. How we do it – have a look!

Manufacturing and lyophilisation of a nanosuspension
Innovative technologies for the development and production of semi-solid and liquid dosage forms are part of our wide range of services in drug development. We will show you the manufacturing of a nanosuspension with subsequent lyophilization under GMP conditions.
Read more … Manufacturing and lyophilisation of a nanosuspension
Media centre - virtual updates

Video: LC-MS in biopharmaceutical analysis
In this update, Professor Franken will explain how LC-MS can be used to investigate the various quality attributes of biopharmaceuticals.
Biopharmaceuticals are drugs that are produced with the help of biotechnology. In contrast to conventional small molecule drugs, which are chemically synthesized, biopharmaceuticals are usually derived from living organisms such as bacteria, yeast or mammalian cells. The structural complexity of protein-based biopharmaceuticals, such as antibodies, requires the use of a wide range of state-of-the-art analytical techniques.
LC-MS in particular is of crucial importance for biopharmaceuticals as it enables detailed analysis of complex molecules. It identifies and quantifies biomolecules and ensures product consistency and safety. Its precision supports quality control and regulatory compliance, making it essential for drug development.