In order to develop a novel compound to a safe and effective treatment, a package of studies is required. These study designs need to be tailored for each compound in development. This requirement is partnered with the need for accurate assessment of safety data, confidence in this data, and often requires delivery within tight timescales.
Our integrated approach helps you move through to IND submission smoothly and cost effectively.
Our Pre-clinical Biosciences group has the expertise and experience to design and execute all of your study requirements and perform them in a single location.
Our Integrated Development includes: