Our research team has over 30 years of experience in the development of finished medicinal products. The scientists bear responsibility not only for creating formulations and substantiating production processes, but also for development and validation of analytical procedures for both investigations during development and for routine quality control of finished products.
The utilisation of modern modelling equipment, in particular, homogenisers, facilitates the correct development, scaling and evaluation of production processes.
The successful realisation of the requisite practical outcomes – most notably, the initiation of the production of pharmaceuticals developed within the institution – is grounded on the presence of specialists with the necessary qualifications, contemporary equipment, scientific methodology and extensive experience.
Main Scientific Directions
- physicochemical studies of disperse systems with a liquid, solid and gaseous dispersion medium (suspensions, emulsions, aerosols, foams, etc.)
- pharmaceutical development and research of finished medicinal products
- development of analytical procedures for support of pharmaceutical development, as well as for quality control of medicines; validation of the analytical procedures
- development / optimisation of production processes with the production of laboratory and/or pilot batches of products
- standardization: preparation of the registration documentation for active pharmaceutical ingredients and finished medicinal products, as well as drafting of scientific guidelines and regulatory documents for pharmaceutical industry in Ukraine