Laboratory of Technology and Analysis of Medicinal Products
Pharmaceutical development, development and validation of analytical procedures for quality control, preparation of regulatory documentation for the pharmaceutical industry
preparations for inhalation (metered dose inhalers)
suppositories
Investigation of inhalation, nasal, and other dosage forms
Study of physicochemical properties of certain medicinal products that are dispersed systems with liquid, solid, or gaseous dispersion media
In vitro release testing to confirm pharmaceutical equivalence
Testing of pressurized metered-dose inhalers and nasal sprays, including aerodynamic particle size distribution (APSD) testing
Stability studies
Analytical support for drug quality: development, validation, and control
Development and validation of analytical methods for drug quality control
Quality control (HPLC, GC, TLC, absorption spectrophotometry in the infrared, ultraviolet, and visible regions, potentiometric titration, particle size distribution by laser diffraction, etc.)