vivoPharm is a contract research organization offering integrated preclinical services in different disease areas to the biotechnology and pharmaceutical industries.
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.
vivoPharm welcomes you to explore our website and to contact us to discuss your needs.
Services
in vivo compound validation and compound profiling in the areas of oncology, angiogenesis and with a partner in CNS.
in vitro compound validation and compound profiling, using semi-throughput manual systems with maximum quality control.
Safety and toxicology studies in our GLP facilities that guarantee an early assessment of toxicokinetic and toxicological profiles in rodents.
Optimized design and timing of pharmacokinetic studies for a smooth transition from in vitro compound profiling to high quality in vivo studies.
Standardized methods or methods tailored for our clients' requirements.
Our highly qualified team of scientists offer a broad range of methods to study biomarkers both in vitro and ex vivo.
Standardized, professional reports and weekly data updates with well annotated tabular data reports.