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CDMO’s fully integrated facility in Suzhou, China was found to conform to EU Eudralex Vol. 4 GMP guidelines
September 10, 2019
By: Tim Wright
Editor-in-Chief, Contract Pharma
CMAB Biopharma (Suzhou) Inc., a pure-play contract development and manufacturing organization (CDMO) specializing in the production of mammalian cell-derived biologic products, received a positive opinion in an external European quality audit conducted by Parexel International Co. The purpose of the audit was to confirm that CMAB’s quality standards are in line with European GMP, thereby verifying that its quality assurance and control systems can meet the requirements of development, pr...
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