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Biopharmaceutical Services

Mobilize the purpose-driven expertise of Covance Biopharmaceutical Services to gain insightful, thorough development of your biotechnology products. With over 250 different molecules successfully supported annually, we now offer you the most comprehensive service in the industry.

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 recombinant proteins, monoclonal antibodies, vaccines, blood products, gene therapy products and more.

In 2010, Covance expanded of its biotechnology offerings into North America with the opening of a new facility on its Greenfield campus in Indiana. This $15 million facility will leverage the expertise developed and offered by Covance in the U.K. for more than 20 years. For more information, please call us or contact your local Covance representative.

Satisfy regulatory and quality compliance statutes with Covance as your development partner.

Quality compliance:

  • GLP, GMP, ISO9001
  • Inspected by MCA, FDA, MHRA for regulatory compliance
  • Regularly inspected by clients

Regulatory compliance:

  • Europe, North America, Japan
  • The International Conference on Harmonisation (ICH)

Customized and committed to clients large or small, Covance recognizes your development program is as unique as the products you bring to our facilities. Streamline testing requirements conform to the latest regulatory guidelines, and satisfy regulatory and quality compliance statutes with Covance.

Greenfield Facility
Dedicated stablity services are one of the offerings from our Greenfield, IN, facility. View the service profile for more information.
State-of-the-Art Facilities

Take a virtual tour of our newly expanded, optimally designed cell banking and biosafety testing facility.

Voice of the Scientist
View a lecture by a Covance scientist discussing Glycoprotein Analysis in Biopharmaceutical Development.
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