Demonstrate your product's safety, efficacy and purity, from preclinical to clinical trial to commercial supplies with Covance. 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 CMC analytical and stability 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, US,  Porcheville, France and Harrogate and Alnwick, UK. Our investment in people, processes and customer service is your reward, because it's yielded an unparalleled combination of laboratories and experience.

For large molecule CMC analytical, development and biotechnology specialty services, please click here.