FDA Requests Comments on Import & Other Compliance Guidance Documents
The Food and Drug Administration is publishing its annual guidance document agenda to seek public comment on possible topics for future guidance document development or revisions of existing ones. Among other things, the Center for Drug Evaluation and Research requests…
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comments on Current Good Manufacturing Practices (CGMPs)/compliance regarding the importation of active pharmaceutical ingredients (API) for use in human drugs and Pre-Launch Activities Importation Requests (PLAIR); and the Center for Food Safety and Applied Nutrition requests comments on its guidance regarding the safety of imported traditional pottery Intended for use with food and the improper use of the terms ‘‘lead free,’’ and the proper identification of ornamental and decorative ware. Comments may be submitted at any time.