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 GMP and other regulatory standards.

The CMC analytical and stability expertise you gain with Covance is built upon 20 years of experience in providing GMP analytical support to the pharmaceutical and biotechnology industries from our facilities in 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 solutions, please click here.


Download our overview brochure on CMC Analytical and Stability Services.

Dedicated Resource Agreement

Click here to find out if Dedicated Resource Agreement (DRA) program is right for you.


Develop, characterize, test and validate with Covance, no matter what technique or molecule you're pursuing. Our experience covers a wide range of biomolecules, including: