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From 3 to 5 December 2014, UFAG Laboratorien AG in Sursee was successfully audited by a representative of the US Food and Drug Administration (FDA).
UFAG LABORATORIEN carries out analytical tests for pharmaceutical clients on products that are approved for the US market and marketed there.
The FDA has a duty to ensure that the legal regulations of the United States (cGMP ) are met. During the inspection at UFAG Laboratorien AG, in addition to a general review of the quality system, a product-specific review of work on a product approved in the United States was also performed.
The commitment of UFAG Laboratorien AG to quality and to the highest possible satisfaction of its partners is confirmed by the successful audit results.