Member of a EUCROF member association

Pharma services

100-200

Pharmaceutical Analyses,Bioanalytical Testing,Clinical Testing,API Solution,Formulation

Quality (CMC) development,Bioequivalence trials,Phase I - IV trials

Healthy men and women,Subjects with renal impairment,Subjects with hepatic impairment,Special population

Validation and transfer of methods,Stability studies,Analyses of highly potent substances,Analyses for validating the production process,Quality control and release analyses,Accelerated stability and degradation studies,In-vitro studies,Biopharmaceutical analyses,Research and Development department,Determination of impurities and their isolation,Analyses of inhalation products,Synthesis and certification of reference materials,Development and validation of bioanalytical methods,BE studies on animals,Analyses of drugs and their metabolites,Determination of structure of metabolites,Biostatistic evaluation,BE study / Phase I study,Pharmacokinetic studies,Toxicokinetic studies (animals),Pharmacodynamic studies,Bioavailability,Bioequivalence studies,Batch linearity,Different modes of administration,Different dosage forms,Steady-state studies,In vitro in vivo correlation,Interactions of drugs and food or alcohol,Influence of diet (before/after eating),Effect of age / gender,Study on a special population,Ethno-bridging studies,Studies on subjects with special health conditions,Registration of generics in Russia,Phase I – IV

Czech Republic,France,Germany,Italy,Russia,South Korea,Spain,United States

We hold GMP, GLP and GCP certifications for human medicinal products and GMP certification for veterinary medicinal products.