cGMP Pharmaceutical Analysis Services
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Demonstrating a product's safety, efficacy and purity to support regulatory submission is the ultimate goal of pharmaceutical product developers and manufacturers. The chemistry, manufacturing and controls process requires flawless analytical data in accordance with cGMP and other regulatory standards.
Covance has over 18 years of experience in providing cGMP analytical support to the pharmaceutical and biotechnology industries at our facilities in Madison, WI and Harrogate, UK.
Our investment in people, process and customer service has yielded an unparalleled combination of laboratories and experience. From small molecules to biologics, clinical trial to commercial supplies, Covance's cGMP pharmaceutical analysis capabilities can help you achieve your drug development and manufacturing goals.
Flexibility and Range of Services
Covance can provide the complete range of services required for your active ingredient and product testing needs including:
We also offer specialized capabilities, such as experience with all dosage forms and delivery systems, nitrosamine analysis and expertise in the evaluation of protein-based products. |
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