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Supplement Manufacturing Practices Survey Proposed By FDA

This article was originally published in The Tan Sheet

Executive Summary

FDA is proposing to conduct a survey of dietary supplement companies' existing manufacturing practices for use in developing its proposed rule on industry-wide GMP standards, the agency says in an Oct. 6 Federal Register notice.

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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.

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

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.

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

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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