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Only 16% Of Supplement Makers Surveyed Report AEs To FDA - GMP Study

This article was originally published in The Tan Sheet

Executive Summary

A scant 37 (16% of 238) dietary supplement establishments that responded to an FDA manufacturing practices survey said they report consumer complaints of adverse events to FDA.

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Supplement GMPs On CFSAN's Autumn "Must Do" List, Levitt Tells CRN

Dietary supplement Good Manufacturing Practices are on the Center for Food Safety & Applied Nutrition's "must do" list for this fall, although a proposed reg will not be issued by the Sept. 30 target deadline, CFSAN Director Joseph Levitt reported.

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