Drive Program Success from the Start
Our experienced team of drug development experts is committed to helping you reach critical decisions faster. With your research goals in mind, we provide study design, nonclinical laboratory selection, and program management solutions to execute a full range of GLP and non-GLP preclinical evaluation studies and advance your program to first-in-human studies.
Advance Seamlessly into the Clinic
Transition into the clinic and set your sights on moving to and through proof of concept with CMC and early clinical support.
Our team brings diverse scientific and drug development expertise in areas including ADME/PK, bioanalysis, CMC, pharmacology, toxicology, and early clinical development. We leverage Premier Consulting’s Quality Management support capabilities to stay at the forefront of quality and compliance standards. We can support both non-regulated exploratory studies as well as regulated studies following GLP, GMP or GCP. The compounds and studies we support include: