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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.
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We provide comprehensive services within clinical trials. 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 any set requirements.
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Analytical services for pre-clinical studies up through Phase III, including statistical evaluation. Comprising 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.

When you provide such a plethora of pharma services it's impossible to list them all, but with countless industry experts and both direct and partner labs available for your project, you can be certain that Conscio can help.