We inspect inspection specifications

Our testing and evaluations are conducted according to Good Manufacturing Practice (GMP) standards, country-specific requirements and your individual specifications. And we go one step further and scrutinize or develop these specifications for you. Based on this, our qualified employee will guarantee that only marketable medicines are put on the market,  so that the path from raw material to final product is profitable and safe – for you as our customer.

Our services
Analyses (layout suitable for authorization documentation)
Method development
Method validation
Method transfer (carried out precisely in accordance with your own requirements or based on our in-house SOPs)
Stability studies (on-going stability tests in accordance with ICH guidelines for various climate zones)
Quality dossiers
Expert reports on quality