The department take part in the scientific work and the QC activity of the Institute.

Methods for analysis are developed, adapted or validated and is prepared analytical documentation for pharmaceutical products. Microbiological control of raw materials, substances and final no sterile dosage forms is performed. The preservative properties of liquid dosage forms, unguents, gels and tooth pastes are determined. Microbiological control of the parameters of the production area and stuff and of the microbiological contamination of the packaging material is done, as well as microbiological validation of the cleaning of the equipment and disinfection of the areas.