Supplement Firms Should Work Toward Sharing GMP Audits – FDA's Williams
This article was originally published in The Tan Sheet
Executive Summary
FDA dietary supplement program official Brad Williams personally endorses the sharing of supplier audit reports to improve firms' compliance with good manufacturing practices.
You may also be interested in...
Convoluted Herbal Requirements Foretell FSMA Complexities
Ingredient importers supplying herbal materials for food and dietary supplement manufacturers will have to consider their downstream customers’ intended uses to comply with FDA regulations under the Food Safety Modernization Act, which are likely to vex many companies.
Convoluted Herbal Requirements Foretell FSMA Complexities
Ingredient importers supplying herbal materials for food and dietary supplement manufacturers will have to consider their downstream customers’ intended uses to comply with FDA regulations under the Food Safety Modernization Act, which are likely to vex many companies.
Interview: Post-FDA, Williams Still Committed To Supplement GMPs
Brad Williams has moved on from FDA’s Division of Dietary Supplement Programs, but he continues to drive industry GMP compliance at NSF International. In an interview, Williams relates what the industry must do to overcome GMP struggles and commends Dan Fabricant’s work as DDSP director.