Aclairo and EPL have the experience and ability to provide consulting services in toxicology and pathology in a cost-effective and timely manner. We will take the time to listen to your needs and coordinate those with availability and appropriate expertise among our staff of consultants.
Our toxicology, nonclinical ADME, and clinical pharmacology consultants have extensive experience in small and large pharmaceutical companies, contract research organizations, FDA, and academia. We can help you design, conduct, monitor, edit, and report your pharmacology and toxicology studies to prepare you for global regulatory success. With expertise in genetic toxicology, general toxicology, carcinogenicity, developmental and reproductive toxicology, and juvenile toxicology, our experts can facilitate product quality assessments (impurities, leachables, excipients) and ADE/OEL to support manufacturing. We can additionally aid the integration of in vitro and in vivo pharmacology and safety pharmacology or abuse liability.
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