News
27.11.2023Renewal as analysis laboratory of the FDA
The CCiTUB have renewed their registration as a Generic Drugs Facility (GDUFA) in the Food and Drug Administration (FDA) as a laboratory for analysis by contract. This registry allows the CCiTUB to perform analysis for companies that wish to sell their products in the North American market. In addition, CCiTUB are audited periodically to verify the compliance of regulations by the companies that analyze products in these facilities.
The FDA information:
DUNS: 473552800
FEI:3009892881
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