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Intertek Pharmaceutical Services aims to mitigate the risks of drug development through the provision of advanced analytical, bioanalytical and characterisation expertise. We offer a broad range of Good Manufacturing Practice (cGMP), Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) compliant laboratory services to clients involved in the development of biologic medicines and advanced therapy medicinal products. Our expertise ensures sufficient information for your filings through expert method development and validation, stability studies and GMP batch release testing. 

With a strong heritage supporting pharmaceutical product development, coupled with a comprehensive range of analytical technology, our experts offer Total Quality Assurance expertise to help you ensure the safety, efficacy and quality of your therapeutic product.

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  • Monitoring of Glycosylation Using Site Specific Approaches


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