FDA Seeks Further Dialogue On Effort To Standardize CMC Application Data Elements

FDA wants feedback on a proposal to standardize the data elements of the quality and chemistry, manufacturing and controls portions of applications. The agency says such a plan will enable consistency in the content and format of CMC data submitted, thus providing a consistent look and feel for every application.

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US FDA said Aug. 22 it wants to hold a public meeting in October on an initiative to streamline the electronic submission of chemistry, manufacturing and controls information in new drug applications using standardized data elements the agency is developing.

The Oct

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