Quality, scientific integrity, cost-effectiveness, and regulatory compliance are essential considerations when selecting an outsourcing partner.
Charles River is adept at balancing these key values within the most stringent timelines to deliver comprehensive GLP/GMP development and manufacturing services from early screening, through preclinical and clinical support, to commercial manufacturing.
Whether you’re seeking to outsource the entirety of your drug development, or simply looking to supplement your own in-house capabilities, our global facilities provide the full-service resources to meet your requirements.