Preclinical Drug Development
Noble Life Sciences provides high-quality, GLP and non-GLP preclinical contract services that help you get from concept to clinic faster and more efficiently. We have a state-of-the-art laboratory facility and vivarium managed by an experienced staff. With our stringent quality control and expertise in cell- & animal-based models, you can trust Noble scientists to help lead and support your drug development programs through each phase of the preclinical process. With proof of concept studies, early safety assessments and other IND enabling services, we are committed to providing a strong scientific foundation to enable your preclinical decisions. We take pride in our ability to successfully customize studies to meet your needs. We will work with you to develop unique procedures and practices to facilitate the research and development of your product.
- Disease & Animal Models
- Drug Pharmacology & Exploratory Toxicology
- Analytical & Laboratory Services
- Oncology Drug Evaluation
- GLP & non-GLP Custom Polyclonal Antibodies
- Tissue Products
- Research Animals
Program Development and Implementation
With extensive and successful experience in drug development, Noble’s scientists can manage your drug development program including design, implementation, and data management. Noble can also develop plans for the management of therapeutic, clinical and business aspects of your drug development program.
We can help you devise a strategy and guide you through your preclinical testing or turn the entire project over to us and we will handle all aspects from protocol to final report.