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Preclinical Laboratory Services
Efficacy & Pharmacology Studies
Validated Cell-Based, Small and Large Animal Models of Human Diseases

Preclinical R&D Services For Pharmaceutical, Medical Device and Diagnostic Development 

MD Biosciences provides comprehensive preclinical efficacy and pharmacology research services to a wide range of industry, academic and government organizations through our Preclinical Laboratory Services Division. At MDB, we pride ourselves on the expertise that our scientific teams have developed over the course of our 25+ year company history. We collaborate with pharmaceutical and biotechnology pioneers to develop innovative animal and cellular models of a variety of complex diseases, with capabilites to run “off-the-shelf” models, customize existing models to meet specific Sponsor needs or develop novel, fit-for-purpose approaches. Our ultimate goal is to be your dedicated research partner for preclinical studies, offering our 100+ years of collective experience in preclinical study design and execution. We work to create a lasting partnership that ensures the most informative and comprehensive data packages possible from each study we perform.


About our Preclinical Laboratory Services:

At MD Biosciences, we offer extensive in vitro, in vivo and ex vivo modeling services for efficacy determinations, PK/PD assessments, mechanism of action studies, compound screening, biomarker analysis, and more! Wherever possible, we emphasize a rigorous, biomarker based approach to every study we run, taking each Sponsor’s unique research objectives into consideration. Our laboratory features multi-parametric (15+ parameters) biomarker and flow cytometry capabilities including BD LSR Fortessa, Western Blotting (Standard & WES by Protein Simple) and ELISA protein analysis. 

Our CRO relationship model includes transparent sharing of information, coordinated decision-making and a high level of flexibility. We utilize thoroughly-validated disease induction methods and positive controls, are fully AAALAC-accredited and GLP-compliant, and have a dedicated Quality Management team to ensure the highest quality data practices are observed. Our knowledgeable staff can support you at each step in the preclinical pipeline, from feasibility assessment, study design, and selection of the appropriate read-outs to final data analysis, reporting and interpretation. 

Contact us today!


Now offering flow cytometric analysis on the BD LSR Fortessa

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+41-44-986 2628