• development and validation of suitable analytical methods to determine active substances in various materials
  • conducting different types of stability studies (accelerated, long-term, intermediate, on-going, in-use, in drinking water) in compliance with the EMA guidelines
  • contract manufacturing of your VMP
    • manufacturing of nonsterile medicinal products, including those containing ampicillins, amoxicillin and sulphonamides (powder dosage forms) in GMP régime
    • premises of D purity class, packaging line
  • secondary packaging