We offer a variety of services in the areas of toxicology and pharmacology to assist companies in the preclinical and clinical development of pharmaceuticals and medical devices and for evaluation of in-licensing and out-licensing opportunities. Areas of expertise include safety assessment of small molecules and biopharmaceuticals, drug metabolism and pharmacokinetics, and biocompatibility analysis for medical devices. These capabilities are supported by a strong in-house (bio)analytical base and formulation capacity.

We cover a comprehensive range of important development activities, including:

• Protocol development
• Study placement, monitoring, and management
• Report writing and full review of the preclinical program
• Design and execution of complete preclinical development programs

Our technical expertise includes:

• Toxicology, including mechanistic studies
• Absorption, Distribution, Metabolism and Excretion (ADME)
• Report writing and full review of the preclinical program
• Pharmacology
• Pharmacokinetics
• Pharmacodynamics