Analysis. Understanding 
the material, safeguarding 
the process.

We systematically determine critical material attributes(CMAs) such as particle size distribution, water activity, and density – using precise methods such as laser diffraction. We also evaluate your material using our Qualified Experts Database (QED), including its processability in relevant steps. This means that even with small quantities of powder, you can assess whether your product is more suitable for a batch-based or continuous process. This creates a sound basis for scalable, efficient, and robust processes.

Our HPLC analytics supply precise reference data for active pharmaceutical ingredients (APIs), impurities, and degradation products – as a complementary component in formulation, process and ePAT development. To ensure that the analytics can be seamlessly integrated into your project, we handle method development and method transfer. This ensures you always have reliable reference values at your disposal without having to rely on external laboratory capacities. The data obtained supports both the development and construction of ePAT models and enables precise process monitoring at a later stage. This provides you with reference analytics from a single source that is reliable, consistently documented, and can be integrated directly into your development process.