FDA takes unprecedented step toward more efficient global pharmaceutical manufacturing inspections 

 

FDA takes unprecedented step toward more efficient global pharmaceutical manufacturing inspections 

 

The U.S. Food and Drug Administration has determined the agency will recognize eight European drug regulatory authorities as capable of conducting inspections of manufacturing facilities that meet FDA requirements. The eight regulatory authorities found to be capable are those located in: Austria, Croatia, France, Italy, Malta, Spain, Sweden and the United Kingdom. Continue reading.

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