Preclincal Concept Validation

vivoPharm is a contract research organization that offers integrated preclinical services in different disease areas to the biotechnology and pharmaceutical industries.

Our team of specialists provides advice and optimized study design to our clients. vivoPharm specializes in conducting tailored studies to guide drug development, starting from compound libraries and ending with a comprehensive set of in vitro and in vivo data and reports, as needed for Investigational New Drug Applications (IND) filing.

vivoPharm operations follow strict quality control methods and meet the highest industrial-standards, acknowledged by our customers world wide. Our highly motivated and qualified team guarantees short response times, consistency of service, regular updates and transparency.

Services

in vitro compound validation and compound profiling, using semi-throughput manual systems with maximum quality control. Optimized design and timing of Pharmacokinetic studies for a smooth transition from in vitro compound profiling to high quality in vivo studies.

in vivo compound validation and compound profiling in the areas of Oncology, Angiogenesis and CNS. vivoPharm has initiated an electronic animal labeling system which guarantees non-biased data acquisition and data processing, as well as long term data security.

Safety and Toxicology studies in our GLP facilities guarantee an early assessment of toxicokinetic and toxicological profiles in rodents.

vivoPharm's ex vivo and pharmacodynamic studies use standardized methods or tailored methods for our clients. Our highly qualified team of scientist offers a broad range of methods to study biomarkers in vitro and ex vivo. We provide standardized professional reports and weekly data updates with well annotated tabular data reports.