Nonclinical Drug Development Services

Meeting project time lines and goals is not a problem with a full complement of experts, such as CCSA's board-certified toxicologists, pharmacologists, chemists, biochemists, microbiologists, nutritionists and other scientists with extensive experience in preclinical research and development. Supporting GLP-required acute, chronic, carcinogenicity, and teratology and reproductive toxicology, as well as short- and long-term efficacy studies, CCSA's scientists provide expertise in design, monitoring, and management of preclinical and nonclincal studies, achieving critical milestones in a timely fashion.

Our Expertise In This Area Includes:

• Strategic and drug development planning
• Customized protocol design development and implementation
• Study monitoring and management
• Study site inspection and qualification
• Study placement and budget oversight
• Regulatory compliance
• Quality assurance and audits
• Data analysis and study report review
• Data management and presentation services
• Report and manuscript preparation