Every Step of the Way.

As a fully integrated partner, Charles River can support your research at any point along the drug discovery continuum.

Model Evaluation Program

A risk-free approach to assessing the quality and compatibility of our animal models. Learn more »

Featured Story

Acquisition Enhances Discovery Research Services

Charles River has completed the acquisition of Argenta and BioFocus from Galapagos NV. This acquisition uniquely positions Charles River as an early-stage CRO with integrated in vitro and in vivo capabilities from target identification and validation through preclinical development. Learn more »

Take a Facility Tour!

Watch video tours of our world-class preclinical facilities. Learn more »

Clinical Support

Supporting your clinical trials with in vivo and in vitro nonclinical studies and clinical-scale manufacturing.

Learn More

The Source℠

Your direct access to our technical, scientific and educational resources.

Register / Log in

Complimentary Webinar

Quality Agreements - A Practical Guide

October 14, 2014 | 1:30 - 2:30 PM EDT
When GMP activities are contracted from one party to another, it is not simply a matter of signing a study plan. Each party has many responsibilities to fulfill in order for the work to be performed correctly; a Quality Agreement is the place to define these responsibilities. Learn more »

Biologics Regulatory Documents Library

Online library of regulatory documents to help you navigate through the development and release process.
Learn more »

Basic Research

Model Evaluation Program

A risk-free approach to assessing the quality and compatibility of our animal models. Learn more »

Drug Discovery

Featured Story

Acquisition Enhances Discovery Research Services

Charles River has completed the acquisition of Argenta and BioFocus from Galapagos NV. This acquisition uniquely positions Charles River as an early-stage CRO with integrated in vitro and in vivo capabilities from target identification and validation through preclinical development. Learn more »

Safety
Assessment

Take a Facility Tour!

Watch video tours of our world-class preclinical facilities. Learn more »

Clinical Development

Clinical Support

Supporting your clinical trials with in vivo and in vitro nonclinical studies and clinical-scale manufacturing.

Learn More

The Source℠

Your direct access to our technical, scientific and educational resources.

Register / Log in

Manufacturing

Complimentary Webinar

Quality Agreements - A Practical Guide

October 14, 2014 | 1:30 - 2:30 PM EDT
When GMP activities are contracted from one party to another, it is not simply a matter of signing a study plan. Each party has many responsibilities to fulfill in order for the work to be performed correctly; a Quality Agreement is the place to define these responsibilities. Learn more »

Biologics Regulatory Documents Library

Online library of regulatory documents to help you navigate through the development and release process.
Learn more »