mypreclinical: Your Global Portal for Effective Study Management
Click here to learn more about mypreclinical, our new and improved global portal. mypreclinical, offers customizable solutions and increased functionality for secure study tracking.
Charles River has the proven experience, range of services and expertise to help you successfully initiate and complete critical phases of preclinical drug development by designing, performing and documenting safety tests that meet the appropriate regulatory requirements before and after clinical trials begin. Our scientific and regulatory preclinical research staff are committed to providing exactly what you need with flexible solutions, accelerated timelines and customized approaches. For your IND-enabling program proposal, click here.
Our preclinical publication, the Researcher, brings readers up to speed on scientific techniques, regulatory considerations and new innovations. Access the Researcher library through our exclusive content portal, The Source℠. To register for The Source℠, please click here. Already registered? Please click here to login.
Related Pathology Services
Our multidisciplinary expertise, state-of-the-art technology and depth of experience with large and small molecules and devices enable us to offer a wide array of integrated pathology services. Click here to learn more.