HomeNewsBusinessCompaniesDrug applications based on Semler's data unacceptable: USFDA

Drug applications based on Semler's data unacceptable: USFDA

The action is being taken as a result of an inspection of Semler's bioanalytical facility in Bangalore conducted between September 29, 2015, and October 9, 2015, USFDA said.

April 22, 2016 / 20:17 IST
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Coming down hard on Semler Research Center over data integrity issues, USFDA has told drug firms that their applications seeking approvals on the basis of studies done by the Bangalore-based firm will not be accepted.

Instead, USFDA said, the firms will need to furnish clinical research by other approved entities.

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"FDA is notifying sponsors of New Drug Applications (NDAs) and Abbreviated New Drug Applications (ANDAs) that clinical and bioanalytical studies conducted by Semler Research Private Ltd are not acceptable as a result of data integrity concerns, and need to be repeated," the United States Food and Drug Administration (USFDA) said in a notification.

The letter informs the sponsor that it must repeat the bioequivalence/bioavailability studies using an entity other than Semler at an acceptable alternate study site, it added.