Department of Pharmaceutics

Department of Pharmaceutics

 

  • Formulation, development and evaluation of human and veterinary dosage forms: main target is preparation of dosage forms with poorly soluble and hardly absorbable APIs; and formulation of dosage forms with controlled release.
  • Innovation and optimization of technological processes: mixing, granulation, pelletization, microparticles preparation, compressing and coating of dosage units.
  • Solid dosage forms:
  • Powders and blends: grinding, micronizing, mixing.
  • Tablets: immediate released (uncoated and coated) and controlled released (matrix and coated).
  • Hard capsules: filling and coating.
  • Pellets: extrusion/spheronization, rotary agglomeration with layering.
  • Microparticles: gelation and evaporation techniques.
  • Mucoadhesives: tablets, multilayer films/patches.
  • Lipid formulations: liquisolid systems, SEDDS, SMEDDS.
  • Liquids and semisolids: Solutions, emulsions, suspensions, ointments, creams, gels, pastes
  • Scale-up and technology transfers.
  • Process validation and IQ, OQ, PQ consultation.
  • Stability studies (performance and evaluation).
  • Preclinical and clinical evaluation (consultation and partnership).
  • Technological documentation – preparing and cooperation (BR, TR, SOP...).
  • Preparation of samples for clinical evaluation (experience - EU, USA, Canada, India).