The US Food and Drug Administration (FDA) on Tuesday released a warning letter sent to Spanish active pharmaceutical ingredient (API) maker Interquim, S.A. for several good manufacturing practices ...
The FDA said in a warning letter that an Indian API maker had not ensured the water it gets from a nearby river is sanitary before using it to make its products. () The FDA has suggested an Indian API ...
The FDA found that a Canadian API maker was not testing the products it shipped to the U.S. (FDA) () An FDA inspector didn’t have to spend long to discover that a Canadian API maker was failing to ...
The US Food and Drug Administration (FDA) on Monday released a warning letter sent to active pharmaceutical ingredient (API) maker Qinhuangdao Zizhu Pharmaceutical for data integrity issues uncovered ...
Mumbai, Oct 12 () Private equity fund PAG is picking up a controlling stake in active pharmaceutical ingredient (API) maker Anjan Drug for over USD 70 million, sources said on Monday. Mumbai, Oct 12 ( ...
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