"Each client is unique and requires an individual approach. Guided by this philosophy, our specialists develop intelligent and 100% efficient multidisciplinary programs in preclinical drug research and chemical safety evaluation"

Serge Richard (CEO)

 

 

 

 

QT shift and probabilistic method: powerful approaches for detection of QT prolongation in a most reliable manner.

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tdpscrren

TDPscreen: a tool invented by CERB for characterization of torsadogenic profiles

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Founded in 1973, CERB has developed to a leading international contract research organization (CRO) in the fields of preclinical pharmacology and toxicology. Taking on the challenges of modern drug development CERB has created its distinctive image of a major service provider to the pharmaceutical industry in the context of innovative biomedical research.

Our toxicology department has also proven to be a valuable partner to other branches, such as chemical and agro-chemical industries, in the field of regulatory safety assessment.

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For the pharmaceutical industry, CERB takes advantage of its sophisticated synergy between pharmacology and toxicology resources to provide complete pre-phase I packages for a new molecule in an economic and timely manner. Having developed/validated more than 100 models and techniques in pharmacology we take on any challenge of specialized approaches fitting the requirements of your compound. A fully equipped chemical analysis unit assures back-up support for drug quantification in chemical or biological matrices as well as biomarker verification.

Our main assets are:

 

  • high quality of scientific and administrative performance
  • continuous innovation through targeted scientific input
  • a network of independent, internationally renowned experts and cooperations
  • the dedication to provide custom-made answers
  • reactivity and flexibility

 

Video

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Experts

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Last publication: "Interferences of the autonomic nervous system with drug induced QT prolongation: a point to consider in non-clinical safety studies"

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NEW: partnership with GENOSAFE for biodistribution studies requested in safety studies of gene transfer vectors

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NEW: partnership with Dr. Vierling Consult for preparation of preclincal documentation (e.g. CTD-Modules 2.4 and 2.6)

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