Conscio Pharma: An innovative and trusted global leader
We have been fully certified top-class service providers to the global pharmaceutical industry for more than twenty-five years. The Conscio Group Pharmaceutical segment consists of companies with specialized areas of expertise and focus.
Pharmaceutical analysis, bioanalytical testing, R&D, clinical studies, and more.
We’re your one stop shop
Validation of analytical methods, quality control, stability studies, batch release and more. The Pharmaceutical analysis department provides analytical services for the pharmaceutical industry, especially in the quality control area. The activities are conducted under Good Manufacturing Practice (GMP) and according to valid ICH guidelines.
We provide comprehensive services within clinical trials (Phase I). Clinical trials include the actual clinical part of a study followed by bioanalytical, pharmacokinetic and statistical evaluation. We specialise in bioequivalence studies (BE), but we are, of course, able to conduct various types of pharmacokinetic or pharmacodynamic studies according to the customer requirements.
Analytical services for pre-clinical studies up through Phase III, including statistical evaluation. Comprising of world-class experts, our team has completed more than 600 bio-studies for pharmaceutical companies, across Europe, the United States, Asia and Australia.
Development of analytical methods, impurities research, degradation studies, trace analyses and more. Using our analytical expertise and state-of-the-art equipment we support clients during their drug development and registration stages following the latest trends in analytical chemistry.
We provide complex analytical services for large molecules, including validation of bioanalytical methods in the GxP environment and method transfer. In addition we offer analytical support to pre-clinical/clinical studies with high molecular weight drugs including the statistical evaluation of pharmaceutical parameters and bioequivalence.
This includes pharmaceutical testing, quality control, and stability testing. We’re also registered and audited by the US FDA, and a holder of the Certificate of GMP Compliance for quality control of Veterinary Medicines in Slovakia.
Testing includes chemical, molecular, biological, ecotoxicological and more. Analyses include solids, liquids, waste, cosmetics, food, common items and much more. Sampling includes waters, wastes, soils, fertilizers and more.
The reagent apparatus checks the raw materials used to prepare medicinal preparations. We can supply reagents and substances for the expansion and renewal of the basic reagent apparatus according to the needs of the pharmacy.
We lead projects to assess the state of the environment and its individual components, conduct activities in the field of waste management, and complete laboratory tests and analyses necessary for the implementation of ecological work.