US FDA Targets Expanding Conduit For Supplement GMP Compliance Information
Gathering GMP information can be as problematic for agency as keeping tabs on all supplements available to US consumers. “Just to be clear, FDA believes we have a data gap in understanding the extent of the dietary supplements in the marketplace,” says ODSP Director Cara Welch.
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Avoid “absolute chaos” and last-minute changes as well as over-reaction responding to FDA officials’ form 483s listing GMP violations found during inspections, says Teresa Gorecki, practice director at Compliance Architects.