Our consultants have extensive experience evaluating and advising on strategic nonclinical pharmacology and toxicology issues including:
Based on our extensive regulatory and contract research organization (CRO) experience, our consultants understand the complex details and timing of studies required by regulatory agencies. While managing your preclinical program, they integrate thorough scientific and regulatory requirements to ensure a robust nonclinical testing strategy. As the interface with your CRO, our consultants can: