Demonstrate your product's safety, efficacy and purity with Covance pharmaceutical analysis services. Your regulatory submissions are supported with flawless data from Covance for the chemistry, manufacturing and controls (CMC) process, assessed in accordance with cGMP and other regulatory standards.

The pharmaceutical analysis expertise you gain with Covance is built upon 20 years of experience in providing cGMP analytical support to the pharmaceutical and biotechnology industries from our facilities in Madison, WI (USA) and Harrogate, UK. Our investment in people, processes and customer service is your reward, because it's yielded an unparalleled combination of laboratories and experience.

From preclinical to clinical trial to commercial supplies, Covance cGMP pharmaceutical analysis capabilities help you achieve your drug development and manufacturing goals, wherever they may be on the drug development paradigm.