PharmaFacts has a unique ability to expand or contract according to your preclinical program needs. Our clients are impressed when they learn about the breadth of our expertise and the efficiency with which we can accommodate their requirements. About small to mid-size biotech companyIs your small to mid-size biotech company behind schedule, overworked, understaffed, and struggling to resource the oversight of preclinical safety study requirements, and manage placement and oversight of studies at CROs in an efficient manner? The demands of managing preclinical drug development, the rapid growth and changes in scientific and regulatory requirements, and the need to have on hand individuals trained in this specialty are all impeding your progress. PharmaFacts is positioned to partner with you to handle virtually any preclinical or nonclinical consulting need.